Canonical Allele Identifier: PA2573074228
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 98215
ClinVar RCV Id: RCV000084524
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364194.1:p.Asn688His
CA225433
NM_001377265.1:c.2062A>C