Canonical Allele Identifier: PA2827664165
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 218258

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339535.1:p.Trp511Leu
CA7033745
NM_001352606.2:c.1532G>T