Canonical Allele Identifier: PA2828932447
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_001369735.1:p.Gly430delinsValCys
CA135371
NM_001382806.1:c.1288_1289insTCT
CA135378
NM_001382806.1:c.1288_1289insTGT
CA135379
NM_001382806.1:c.1288_1289insTTT
CA2733207352
NM_001382806.1:c.1288_1289insTAT