Allele Registry

Canonical Allele Identifier: PA107498

Gene: MYL2 HGNC NCBI

ClinVar RCV:

RCV000015112

RCV000246859

RCV002247340

RCV002504789

ClinVar Variation:

14068

HGVS (amino-acid)	Matching Registered Transcripts
NP_000423.2:p.Phe18Leu	CA010488 NM_000432.4:c.52T>C CA386700275 NM_000432.4:c.54C>G CA386700276 NM_000432.4:c.54C>A