Canonical Allele Identifier: PA2825653998
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1426554
ClinVar RCV Id: RCV001933417

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121164.1:p.Lys359Arg
CA7033518
NM_001127692.3:c.1076A>G