Canonical Allele Identifier: PA915977292
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14252
ClinVar RCV Id: RCV000015321 RCV000084548
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116538.2:p.Val672Met
CA225483
NM_001123066.4:c.2014G>A