Canonical Allele Identifier: PA2580402157
Gene: TMEM106B HGNC NCBI

Linked Data

ClinVar Variation Id: 1925499
ClinVar RCV Id: RCV002626009
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060844.2:p.Ile187Val
CA4165133
NM_018374.4:c.559A>G