Allele Registry

Canonical Allele Identifier: PA130591

Gene: TMEM231 HGNC NCBI

ClinVar Allele:

48420

ClinVar RCV:

RCV000033041

RCV001778672

RCV002513310

ClinVar Variation:

39821

HGVS (amino-acid)	Matching Registered Transcripts
NP_001070884.2:p.Met25Lys	CA130590 NM_001077416.2:c.74T>A