Allele Registry

Canonical Allele Identifier: PA2828682421

Gene: TMEM181 HGNC NCBI

ClinVar RCV:

RCV004072415

ClinVar Variation:

2204988

HGVS (amino-acid)	Matching Registered Transcripts
NP_001363783.1:p.Tyr384Cys	CA4073610 NM_001376854.1:c.1151A>G