Canonical Allele Identifier: PA2830303322
Gene: TMEM237 HGNC NCBI

Linked Data

ClinVar Variation Id: 286946

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689601.2:p.Val356Met
CA2056302
NM_152388.4:c.1066G>A