Allele Registry

Canonical Allele Identifier: PA645488772

Gene: TMEM237 HGNC NCBI

ClinVar RCV:

RCV000243342

RCV000402180

RCV000986978

ClinVar Variation:

257313

HGVS (amino-acid)	Matching Registered Transcripts
NP_001037850.1:p.Asn342Asp	CA2056327 NM_001044385.3:c.1024A>G