Allele Registry

Canonical Allele Identifier: PA107509

Gene: MYL2 HGNC NCBI

ClinVar RCV:

RCV000015110

RCV003996096

ClinVar Variation:

14066

HGVS (amino-acid)	Matching Registered Transcripts
NP_000423.2:p.Pro95Ala	CA010047 NM_000432.4:c.283C>G