Canonical Allele Identifier: PA2825653900
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 218252

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121164.1:p.Gln267Arg
CA10575828
NM_001127692.3:c.800A>G