Allele Registry

Canonical Allele Identifier: PA144707

Gene: TMEM231 HGNC NCBI

ClinVar RCV:

RCV000054807

RCV003387749

ClinVar Variation:

64620

HGVS (amino-acid)	Matching Registered Transcripts
NP_001070884.2:p.Gln325Pro	CA144706 NM_001077416.2:c.974A>C