Canonical Allele Identifier: PA2573175867
Gene: TMEM237 HGNC NCBI

Linked Data

ClinVar Variation Id: 1346033
ClinVar RCV Id: RCV002029805

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001037850.1:p.Val360Leu
CA350304627
NM_001044385.3:c.1078G>T
CA350304629
NM_001044385.3:c.1078G>C