Allele Registry

Canonical Allele Identifier: PA2830302973

Gene: TMEM237 HGNC NCBI

ClinVar Allele:

359341

ClinVar RCV:

RCV000413936

RCV000945894

ClinVar Variation:

373720

HGVS (amino-acid)	Matching Registered Transcripts
NP_689601.2:p.Arg25Cys	CA2056583 NM_152388.4:c.73C>T