Canonical Allele Identifier: PA135377
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_004439.2:p.Gly776delinsValCys
CA135371
NM_004448.4:c.2326_2327insTCT
CA135378
NM_004448.4:c.2326_2327insTGT
CA135379
NM_004448.4:c.2326_2327insTTT
CA2733207352
NM_004448.4:c.2326_2327insTAT