Allele Registry

Canonical Allele Identifier: PA276959

Gene: OCA2 HGNC NCBI

ClinVar RCV:

RCV000192364

ClinVar Variation:

211767

HGVS (amino-acid)	Matching Registered Transcripts
NP_000266.2:p.Asn476Ser	CA276958 NM_000275.3:c.1427A>G