Canonical Allele Identifier: PA2827666688
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 218258

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339541.1:p.Trp196Leu
CA7033745
NM_001352612.2:c.587G>T