Allele Registry

Canonical Allele Identifier: PA2827384696

Gene: MYO18A HGNC NCBI

ClinVar Allele:

2213190

ClinVar RCV:

RCV004085419

ClinVar Variation:

2218538

HGVS (amino-acid)	Matching Registered Transcripts
NP_001333696.1:p.Tyr482Cys	CA398467514 NM_001346767.2:c.1445A>G