Canonical Allele Identifier: PA2573074225
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_001364194.1:p.Gly664Val
CA225421
NM_001377265.1:c.1991G>T