Allele Registry

Canonical Allele Identifier: PA129428

Gene: MYH14 HGNC NCBI

ClinVar RCV:

RCV000023718

RCV003228899

ClinVar Variation:

30739

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139281.1:p.Arg974Leu	CA129426 NM_001145809.2:c.2921G>T