Canonical Allele Identifier: PA2825450191
Gene: TMEM231 HGNC NCBI

Linked Data

ClinVar Variation Id: 380471
ClinVar RCV Id: RCV000878632 RCV001703598 RCV003959891 RCV004022329
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070886.1:p.Asp240Gly
CA8176061
NM_001077418.3:c.719A>G