Allele Registry

Canonical Allele Identifier: PA2830303299

Gene: TMEM237 HGNC NCBI

ClinVar Variation Id: 257313

HGVS (amino-acid)	Matching Registered Transcripts
NP_689601.2:p.Asn334Asp	CA2056327 NM_152388.4:c.1000A>G