Canonical Allele Identifier: PA645488819
Gene: TMEM237 HGNC NCBI

Linked Data

ClinVar Variation Id: 286946
ClinVar RCV Id: RCV000290466 RCV001079934 RCV003920116
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001037850.1:p.Val364Met
CA2056302
NM_001044385.3:c.1090G>A