Canonical Allele Identifier: PA107434
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 218258

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000273.2:p.Trp559Leu
CA7033745
NM_000282.4:c.1676G>T