Canonical Allele Identifier: PA2825653932
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 498769

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121164.1:p.Met290Arg
CA388694737
NM_001127692.3:c.869T>G