Allele Registry

Canonical Allele Identifier: PA261388

Gene: MYL2 HGNC NCBI

ClinVar Allele:

52631

ClinVar RCV:

RCV000036387

RCV000484012

RCV002433497

ClinVar Variation:

43461

HGVS (amino-acid)	Matching Registered Transcripts
NP_000423.2:p.Gly87Ala	CA009968 NM_000432.4:c.260G>C