Canonical Allele Identifier: PA645486029
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_001070884.2:p.Asp293Gly
CA8176061
NM_001077416.2:c.878A>G