Canonical Allele Identifier: PA2825450168
Gene: TMEM231 HGNC NCBI

Linked Data

ClinVar Variation Id: 64619
ClinVar RCV Id: RCV000054806 RCV000162154 RCV001781386 RCV003915018 RCV003987343 RCV003764728
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070886.1:p.Val222Ile
CA144704
NM_001077418.3:c.664G>A