Canonical Allele Identifier: PA2580147144
Gene: TMEM237 HGNC NCBI

Linked Data

ClinVar Variation Id: 1906010
ClinVar RCV Id: RCV002583938
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001037850.1:p.Glu351Lys
CA2056308
NM_001044385.3:c.1051G>A