Canonical Allele Identifier: PA658655039
Gene: TMEM231 HGNC NCBI

Linked Data

ClinVar Variation Id: 445818
ClinVar RCV Id: RCV000515034 RCV001003228 RCV001865689 RCV003222011
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070884.2:p.Leu134Phe
CA8176255
NM_001077416.2:c.400C>T