Canonical Allele Identifier: PA2828703717
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14246
ClinVar RCV Id: RCV000015315 RCV000084519
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364195.1:p.Gly598Val
CA225421
NM_001377266.1:c.1793G>T