Canonical Allele Identifier: PA658802129
Gene: TMEM231 HGNC NCBI

Linked Data

ClinVar Variation Id: 499740
ClinVar RCV Id: RCV000593061 RCV002065162 RCV003160029
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070884.2:p.Arg303Gln
CA8176052
NM_001077416.2:c.908G>A