Allele Registry

Canonical Allele Identifier: PA2825776917

Gene: TMEM106B HGNC NCBI

ClinVar RCV:

RCV001872532

ClinVar Variation:

1360573

HGVS (amino-acid)	Matching Registered Transcripts
NP_001127704.1:p.Met192Ile	CA366857332 NM_001134232.2:c.576G>A CA366857333 NM_001134232.2:c.576G>C CA366857334 NM_001134232.2:c.576G>T