Allele Registry

Canonical Allele Identifier: PA2828682355

Gene: TMEM181 HGNC NCBI

ClinVar RCV:

RCV004072415

ClinVar Variation:

2204988

HGVS (amino-acid)	Matching Registered Transcripts
NP_001363779.1:p.Tyr419Cys	CA4073610 NM_001376850.1:c.1256A>G