Canonical Allele Identifier: PA312811
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 203875

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000273.2:p.Leu146Pro
CA312810
NM_000282.4:c.437T>C