Canonical Allele Identifier: PA2830303314
Gene: TMEM237 HGNC NCBI

Linked Data

ClinVar Variation Id: 499112
ClinVar RCV Id: RCV000597448

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689601.2:p.Asn354Lys
CA350304578
NM_152388.4:c.1062T>G
CA350304580
NM_152388.4:c.1062T>A