Allele Registry

Canonical Allele Identifier: PA645495320

Gene: MYH2 HGNC NCBI

ClinVar RCV:

RCV000455902

RCV000490432

RCV001723786

ClinVar Variation:

225415

HGVS (amino-acid)	Matching Registered Transcripts
NP_060004.3:p.Val805Ala	CA8391132 NM_017534.6:c.2414T>C