Canonical Allele Identifier: PA2826131593
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 449078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171475.1:p.Lys298Arg
CA388694612
NM_001178004.2:c.893A>G