Allele Registry

Canonical Allele Identifier: PA252136

Gene: MYH14 HGNC NCBI

ClinVar RCV:

RCV000002282

ClinVar Variation:

2198

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139281.1:p.Arg767Ser	CA252135 NM_001145809.2:c.2299C>A