Canonical Allele Identifier: PA2826131678
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 2130507
ClinVar RCV Id: RCV003052115

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171475.1:p.Val376Ala
CA388695227
NM_001178004.2:c.1127T>C