Canonical Allele Identifier: PA2827665137
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 459939

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339537.1:p.Glu235Gly
CA388694346
NM_001352608.2:c.704A>G