Canonical Allele Identifier: PA225425
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14253
ClinVar RCV Id: RCV000015322 RCV000084521 RCV000763404
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_058518.1:p.Asn221Lys
CA225424
NM_016834.5:c.663T>G
CA399983169
NM_016834.5:c.663T>A