Allele Registry

Canonical Allele Identifier: PA2828682391

Gene: TMEM181 HGNC NCBI

ClinVar RCV:

RCV004072415

ClinVar Variation:

2204988

HGVS (amino-acid)	Matching Registered Transcripts
NP_001363781.1:p.Tyr411Cys	CA4073610 NM_001376852.1:c.1232A>G