Canonical Allele Identifier: PA645488721
Gene: TMEM237 HGNC NCBI

Linked Data

ClinVar Variation Id: 373720
ClinVar RCV Id: RCV000413936 RCV000945894
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001037850.1:p.Arg33Cys
CA2056583
NM_001044385.3:c.97C>T