Canonical Allele Identifier: PA2825653905
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 449078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121164.1:p.Lys272Arg
CA388694612
NM_001127692.3:c.815A>G