Canonical Allele Identifier: PA2827664821
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 38865

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339536.1:p.Val525Phe
CA292687
NM_001352607.2:c.1573G>T