Canonical Allele Identifier: PA2828930919
Gene: ERBB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 44987
ClinVar RCV Id: RCV000038126
ClinVar Variation Id: 44988
ClinVar RCV Id: RCV000038127 RCV000431743
ClinVar Variation Id: 44989
ClinVar RCV Id: RCV000038128
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369731.1:p.Gly690delinsValCys
CA135371
NM_001382802.1:c.2068_2069insTCT
CA135378
NM_001382802.1:c.2068_2069insTGT
CA135379
NM_001382802.1:c.2068_2069insTTT
CA2733207352
NM_001382802.1:c.2068_2069insTAT