Canonical Allele Identifier: PA2826131556
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 459939

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171475.1:p.Glu261Gly
CA388694346
NM_001178004.2:c.782A>G