Canonical Allele Identifier: PA2828925929
Gene: ERBB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 44987
ClinVar RCV Id: RCV000038126
ClinVar Variation Id: 44988
ClinVar Variation Id: 44989
ClinVar RCV Id: RCV000038128

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369721.1:p.Gly764delinsValCys
CA135371
NM_001382792.1:c.2290_2291insTCT
CA135378
NM_001382792.1:c.2290_2291insTGT
CA135379
NM_001382792.1:c.2290_2291insTTT
CA2733207352
NM_001382792.1:c.2290_2291insTAT