Allele Registry

Canonical Allele Identifier: PA2827664585

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_001339536.1:p.Ser279Arg	CA388694657 NM_001352607.2:c.835A>C CA388694672 NM_001352607.2:c.837C>A CA388694673 NM_001352607.2:c.837C>G