Canonical Allele Identifier: PA2825654261
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 218266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121164.1:p.Gly642Arg
CA7033866
NM_001127692.3:c.1924G>A
CA388640367
NM_001127692.3:c.1924G>C