Canonical Allele Identifier: PA2826131838
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 38865
ClinVar RCV Id: RCV000032108 RCV000127322 RCV002262596
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171475.1:p.Val551Phe
CA292687
NM_001178004.2:c.1651G>T