Canonical Allele Identifier: PA2828703378
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 1335279
ClinVar RCV Id: RCV001815827 RCV001869641
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364194.1:p.Glu9Lys
CA8617496
NM_001377265.1:c.25G>A