Allele Registry

Canonical Allele Identifier: PA2826986599

Gene: MYO18B HGNC NCBI

ClinVar RCV:

RCV001673433

RCV001779299

ClinVar Variation:

1256824

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305174.1:p.Trp661Arg	CA10160021 NM_001318245.2:c.1981T>C CA410992843 NM_001318245.2:c.1981T>A