Canonical Allele Identifier: PA915977308
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 98231
ClinVar RCV Id: RCV000084551 RCV000692998 RCV003905079
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116538.2:p.Val698Ile
CA225490
NM_001123066.4:c.2092G>A