Canonical Allele Identifier: PA2573074232
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14254
ClinVar RCV Id: RCV000015323 RCV000084530
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364194.1:p.Ser697Asn
CA225453
NM_001377265.1:c.2090G>A