Allele Registry

Canonical Allele Identifier: PA181065

Gene: MYL2 HGNC NCBI

ClinVar RCV:

RCV000489222

RCV001297385

RCV002399541

RCV003998256

ClinVar Variation:

177958

HGVS (amino-acid)	Matching Registered Transcripts
NP_000423.2:p.Ala55Ser	CA009898 NM_000432.4:c.163G>T