Canonical Allele Identifier: PA2825776914
Gene: TMEM106B HGNC NCBI

Linked Data

ClinVar Variation Id: 1925499
ClinVar RCV Id: RCV002626009

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127704.1:p.Ile187Val
CA4165133
NM_001134232.2:c.559A>G