Canonical Allele Identifier: PA645389306
Gene: TMEM231 HGNC NCBI

Linked Data

ClinVar Variation Id: 380470
ClinVar RCV Id: RCV000952419 RCV001703597 RCV002524875
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070886.1:p.Leu3Val
CA8176321
NM_001077418.3:c.7C>G