Canonical Allele Identifier: PA155726
Gene: TMEM237 HGNC NCBI

Linked Data

ClinVar Variation Id: 130592
ClinVar RCV Id: RCV000118633 RCV000345380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689601.2:p.Ala358Ser
CA155725
NM_152388.4:c.1072G>T