Allele Registry

Canonical Allele Identifier: PA2830092011

Gene: MYO18B HGNC NCBI

ClinVar RCV:

RCV001648280

ClinVar Variation:

1244014

HGVS (amino-acid)	Matching Registered Transcripts
NP_115997.5:p.Ser1444Thr	CA10160853 NM_032608.6:c.4330T>A