Allele Registry

Canonical Allele Identifier: PA105885

Gene: MYH8 HGNC NCBI

ClinVar RCV:

RCV000015197

RCV000015198

RCV000438123

ClinVar Variation:

14136

HGVS (amino-acid)	Matching Registered Transcripts
NP_002463.2:p.Arg674Gln	CA123752 NM_002472.3:c.2021G>A