Canonical Allele Identifier: PA2580147619
Gene: TMEM231 HGNC NCBI

Linked Data

ClinVar Variation Id: 2189147
ClinVar RCV Id: RCV002636724

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070884.2:p.Ser26Asn
CA396810714
NM_001077416.2:c.77G>A