Canonical Allele Identifier: PA2826131712
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 662772
ClinVar RCV Id: RCV000820501

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171475.1:p.Arg399Trp
CA388695371
NM_001178004.2:c.1195C>T