Canonical Allele Identifier: PA2825450004
Gene: TMEM231 HGNC NCBI

Linked Data

ClinVar Variation Id: 516700
ClinVar RCV Id: RCV000607297 RCV000878633 RCV002528745
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070886.1:p.Ala32Val
CA8176304
NM_001077418.3:c.95C>T