Canonical Allele Identifier: PA225428
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_001116538.2:p.Asn614Lys
CA225424
NM_001123066.4:c.1842T>G
CA399983169
NM_001123066.4:c.1842T>A