Canonical Allele Identifier: PA2826131814
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 429410

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171475.1:p.Ser520Cys
CA7033719
NM_001178004.2:c.1558A>T