Canonical Allele Identifier: PA2580402159
Gene: TMEM106B HGNC NCBI

Linked Data

ClinVar Variation Id: 2413950
ClinVar RCV Id: RCV003106283

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060844.2:p.Met192Lys
CA366857324
NM_018374.4:c.575T>A