Allele Registry

Canonical Allele Identifier: PA096578

Gene: TMEM231 HGNC NCBI

ClinVar Allele:

48421

ClinVar RCV:

RCV000033042

RCV000255979

RCV000543480

RCV002513311

RCV003155046

ClinVar Variation:

39822

HGVS (amino-acid)	Matching Registered Transcripts
NP_001070886.1:p.Asp209Asn	CA130593 NM_001077418.3:c.625G>A