Canonical Allele Identifier: PA2830303331
Gene: TMEM237 HGNC NCBI

Linked Data

ClinVar Variation Id: 333560
ClinVar RCV Id: RCV000290602
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689601.2:p.Ser364Cys
CA10612433
NM_152388.4:c.1091C>G