Allele Registry

Canonical Allele Identifier: PA114620

Gene: CA2 HGNC NCBI

ClinVar RCV:

RCV000000961

RCV000328868

RCV000961873

ClinVar Variation:

913

HGVS (amino-acid)	Matching Registered Transcripts
NP_000058.1:p.Asn252Asp	CA114619 NM_000067.3:c.754A>G