Canonical Allele Identifier: PA2825450213
Gene: TMEM231 HGNC NCBI

Linked Data

ClinVar Variation Id: 2041174
ClinVar RCV Id: RCV002912908
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070886.1:p.Met265Val
CA8176019
NM_001077418.3:c.793A>G