Canonical Allele Identifier: PA2573175871
Gene: TMEM237 HGNC NCBI

Linked Data

ClinVar Variation Id: 1360827
ClinVar RCV Id: RCV001907212
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001037850.1:p.Ser385Asn
CA350304112
NM_001044385.3:c.1154G>A