Canonical Allele Identifier: PA2825450014
Gene: TMEM231 HGNC NCBI

Linked Data

ClinVar Variation Id: 2108766
ClinVar RCV Id: RCV003017722

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070886.1:p.His46Pro
CA396809997
NM_001077418.3:c.137A>C