Allele Registry

Canonical Allele Identifier: PA296964

Gene: MYL2 HGNC NCBI

ClinVar RCV:

RCV001219554

RCV002390384

RCV003532001

RCV003998371

ClinVar Variation:

181428

HGVS (amino-acid)	Matching Registered Transcripts
NP_000423.2:p.Ile35Val	CA009829 NM_000432.4:c.103A>G