Allele Registry

Canonical Allele Identifier: PA645488721

Gene: TMEM237 HGNC NCBI

ClinVar Allele:

359341

ClinVar RCV:

RCV000413936

RCV000945894

ClinVar Variation:

373720

HGVS (amino-acid)	Matching Registered Transcripts
NP_001037850.1:p.Arg33Cys	CA2056583 NM_001044385.3:c.97C>T