Canonical Allele Identifier: PA2827663549
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 38865

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339534.1:p.Val551Phe
CA292687
NM_001352605.2:c.1651G>T