Allele Registry

Canonical Allele Identifier: PA096590

Gene: TMEM231 HGNC NCBI

ClinVar Allele:

75584

ClinVar RCV:

RCV000054807

RCV003387749

ClinVar Variation:

64620

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