Allele Registry

Canonical Allele Identifier: PA2499248099

Gene: MYO18B HGNC NCBI

ClinVar RCV:

RCV001648280

ClinVar Variation:

1244014

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305174.1:p.Ser1445Thr	CA10160853 NM_001318245.2:c.4333T>A