Allele Registry

Canonical Allele Identifier: PA153831

Gene: MYH8 HGNC NCBI

ClinVar RCV:

RCV000117692

RCV000341726

RCV001647133

ClinVar Variation:

129678

HGVS (amino-acid)	Matching Registered Transcripts
NP_002463.2:p.Trp1692Arg	CA153830 NM_002472.3:c.5074T>C CA398094961 NM_002472.3:c.5074T>A