Canonical Allele Identifier: PA2825654149
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 38865

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121164.1:p.Val525Phe
CA292687
NM_001127692.3:c.1573G>T