Canonical Allele Identifier: PA2826131590
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 2137535
ClinVar RCV Id: RCV003062605

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171475.1:p.Gln293Glu
CA388694573
NM_001178004.2:c.877C>G