Canonical Allele Identifier: PA2826131688
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1426554
ClinVar RCV Id: RCV001933417

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171475.1:p.Lys385Arg
CA7033518
NM_001178004.2:c.1154A>G