Allele Registry

Canonical Allele Identifier: PA2580206527

Gene: MYO18A HGNC NCBI

ClinVar Allele:

2213190

ClinVar RCV:

RCV004085419

ClinVar Variation:

2218538

HGVS (amino-acid)	Matching Registered Transcripts
NP_001333695.1:p.Tyr494Cys	CA398467514 NM_001346766.2:c.1481A>G