Canonical Allele Identifier: PA2828928476
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_001369726.1:p.Gly743delinsValCys
CA135371
NM_001382797.1:c.2227_2228insTCT
CA135378
NM_001382797.1:c.2227_2228insTGT
CA135379
NM_001382797.1:c.2227_2228insTTT
CA2733207352
NM_001382797.1:c.2227_2228insTAT