Canonical Allele Identifier: PA915963894
Gene: TMEM231 HGNC NCBI

Linked Data

ClinVar Variation Id: 473321
ClinVar RCV Id: RCV000555326 RCV001712516 RCV001821602
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070886.1:p.Asp309_Leu310delinsGluVal
CA658656514
NM_001077418.3:c.927_928delinsAG