Allele Registry

Canonical Allele Identifier: PA2499293658

Gene: MYO18B HGNC NCBI

ClinVar RCV:

RCV001620895

RCV001779268

ClinVar Variation:

1232547

HGVS (amino-acid)	Matching Registered Transcripts
NP_115997.5:p.Trp547Cys	CA10159903 NM_032608.6:c.1641G>C CA411005667 NM_032608.6:c.1641G>T