Canonical Allele Identifier: PA2827665937
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1490406
ClinVar RCV Id: RCV001983721

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339539.1:p.Arg84Leu
CA388695374
NM_001352610.2:c.251G>T