Canonical Allele Identifier: PA2573275733
Gene: TMEM106B HGNC NCBI

Linked Data

ClinVar Variation Id: 1360573
ClinVar RCV Id: RCV001872532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060844.2:p.Met192Ile
CA366857332
NM_018374.4:c.576G>A
CA366857333
NM_018374.4:c.576G>C
CA366857334
NM_018374.4:c.576G>T