Allele Registry

Canonical Allele Identifier: PA2826836692

Gene: CA2 HGNC NCBI

ClinVar RCV:

RCV000000961

RCV000328868

RCV000961873

ClinVar Variation:

913

HGVS (amino-acid)	Matching Registered Transcripts
NP_001280604.1:p.Asn151Asp	CA114619 NM_001293675.2:c.451A>G