Canonical Allele Identifier: PA135393
Gene: ERBB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 44991
ClinVar Variation Id: 376036
ClinVar RCV Id: RCV000439788

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004439.2:p.Val777Leu
CA135387
NM_004448.4:c.2329G>T
CA16602503
NM_004448.4:c.2329G>C