Canonical Allele Identifier: PA916066022
Gene: TMEM106B HGNC NCBI

Linked Data

ClinVar Variation Id: 523236
ClinVar RCV Id: RCV000626490 RCV001561829
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060844.2:p.Asp252Asn
CA366858893
NM_018374.4:c.754G>A