Allele Registry

Canonical Allele Identifier: PA2830091648

Gene: MYO18B HGNC NCBI

ClinVar RCV:

RCV001695224

RCV001779319

ClinVar Variation:

1280072

HGVS (amino-acid)	Matching Registered Transcripts
NP_115997.5:p.His1119Gln	CA10160531 NM_032608.6:c.3357C>A CA410998098 NM_032608.6:c.3357C>G