Allele Registry

Canonical Allele Identifier: PA2826986531

Gene: MYO18B HGNC NCBI

ClinVar RCV:

RCV001620895

RCV001779268

ClinVar Variation:

1232547

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305174.1:p.Trp547Cys	CA10159903 NM_001318245.2:c.1641G>C CA411005667 NM_001318245.2:c.1641G>T