Canonical Allele Identifier: PA096590
Gene: TMEM231 HGNC NCBI

Linked Data

ClinVar Variation Id: 64620
ClinVar RCV Id: RCV000054807 RCV003387749
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070886.1:p.Gln272Pro
CA144706
NM_001077418.3:c.815A>C