Canonical Allele Identifier: PA2825776916
Gene: TMEM106B HGNC NCBI

Linked Data

ClinVar Variation Id: 2413950
ClinVar RCV Id: RCV003106283
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127704.1:p.Met192Lys
CA366857324
NM_001134232.2:c.575T>A