Canonical Allele Identifier: PA225456
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_005901.2:p.Ser305Asn
CA225453
NM_005910.6:c.914G>A