Canonical Allele Identifier: PA225422
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14246
ClinVar RCV Id: RCV000015315 RCV000084519
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005901.2:p.Gly272Val
CA225421
NM_005910.6:c.815G>T