Allele Registry

Canonical Allele Identifier: PA2828682461

Gene: TMEM181 HGNC NCBI

ClinVar RCV:

RCV004072415

ClinVar Variation:

2204988

HGVS (amino-acid)	Matching Registered Transcripts
NP_001363785.1:p.Tyr330Cys	CA4073610 NM_001376856.1:c.989A>G