Canonical Allele Identifier: PA658807079
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_001127704.1:p.Asp252Asn
CA366858893
NM_001134232.2:c.754G>A