Allele Registry

Canonical Allele Identifier: PA2828682442

Gene: TMEM181 HGNC NCBI

ClinVar RCV:

RCV004072415

ClinVar Variation:

2204988

HGVS (amino-acid)	Matching Registered Transcripts
NP_001363784.1:p.Tyr379Cys	CA4073610 NM_001376855.1:c.1136A>G