Canonical Allele Identifier: PA100526
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_058519.3:p.Pro618Ser
CA225439
NM_016835.5:c.1852C>T