Canonical Allele Identifier: PA2826131844
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 218258

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171475.1:p.Trp559Leu
CA7033745
NM_001178004.2:c.1676G>T