Allele Registry

Canonical Allele Identifier: PA2573066205

Gene: MYH14 HGNC NCBI

ClinVar RCV:

RCV001765235

ClinVar Variation:

1305060

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139281.1:p.Arg767Cys	CA406944924 NM_001145809.2:c.2299C>T