Allele Registry

Canonical Allele Identifier: PA273200

Gene: MYL2 HGNC NCBI

ClinVar Allele:

175531

ClinVar RCV:

RCV000151360

ClinVar Variation:

164469

HGVS (amino-acid)	Matching Registered Transcripts
NP_000423.2:p.His161Arg	CA010425 NM_000432.4:c.482A>G