Canonical Allele Identifier: PA144705
Gene: TMEM231 HGNC NCBI

Linked Data

ClinVar Variation Id: 64619
ClinVar RCV Id: RCV000054806 RCV000162154 RCV001781386 RCV003915018 RCV003987343 RCV003764728
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070884.2:p.Val275Ile
CA144704
NM_001077416.2:c.823G>A