Canonical Allele Identifier: PA2827666406
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 218258

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339540.1:p.Trp244Leu
CA7033745
NM_001352611.2:c.731G>T