Canonical Allele Identifier: PA658678987
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 459937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000273.2:p.Val673Leu
CA7033870
NM_000282.4:c.2017G>C