Allele Registry

Canonical Allele Identifier: PA129427

Gene: MYH14 HGNC NCBI

ClinVar RCV:

RCV000023718

RCV003228899

ClinVar Variation:

30739

HGVS (amino-acid)	Matching Registered Transcripts
NP_001070654.1:p.Arg941Leu	CA129426 NM_001077186.2:c.2822G>T