Canonical Allele Identifier: PA2827664159
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 38865

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339535.1:p.Val503Phe
CA292687
NM_001352606.2:c.1507G>T