Canonical Allele Identifier: PA916010389
Gene: ACTN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 216494

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265272.1:p.Ser885Pro
CA338853
NM_001278343.2:c.2653T>C