Canonical Allele Identifier: PA916035565
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 429410

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339538.1:p.Ser520Cys
CA7033719
NM_001352609.2:c.1558A>T