Canonical Allele Identifier: PA645486031
Gene: TMEM231 HGNC NCBI

Linked Data

ClinVar Variation Id: 285611
ClinVar RCV Id: RCV000387372 RCV000650604
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070884.2:p.Phe296Leu
CA8176057
NM_001077416.2:c.886T>C
CA396804318
NM_001077416.2:c.888T>A
CA396804320
NM_001077416.2:c.888T>G