Allele Registry

Canonical Allele Identifier: PA107467

Gene: MYL2 HGNC NCBI

ClinVar RCV:

RCV000015111

RCV000157369

RCV000158923

RCV000621867

RCV000844711

RCV001798005

ClinVar Variation:

14067

HGVS (amino-acid)	Matching Registered Transcripts
NP_000423.2:p.Arg58Gln	CA009915 NM_000432.4:c.173G>A