Canonical Allele Identifier: PA658678969
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 449078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000273.2:p.Lys298Arg
CA388694612
NM_000282.4:c.893A>G