Canonical Allele Identifier: PA225442
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14256
ClinVar RCV Id: RCV000015325 RCV000084526
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005901.2:p.Pro301Ser
CA225439
NM_005910.6:c.901C>T