Allele Registry

Canonical Allele Identifier: PA891845415

Gene: PCCA HGNC NCBI

ClinVar Variation Id: 568261

ClinVar RCV Id: RCV000688562

ClinVar Variation Id: 2802054

ClinVar RCV Id: RCV003624847

HGVS (amino-acid)	Matching Registered Transcripts
NP_000273.2:p.Ser305Arg	CA388694657 NM_000282.4:c.913A>C CA388694672 NM_000282.4:c.915C>A CA388694673 NM_000282.4:c.915C>G