Canonical Allele Identifier: PA2825450228
Gene: TMEM231 HGNC NCBI

Linked Data

ClinVar Variation Id: 2042720
ClinVar RCV Id: RCV002908141 RCV002908142
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070886.1:p.Ile289Val
CA8176006
NM_001077418.3:c.865A>G