Canonical Allele Identifier: PA100546
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14262
ClinVar RCV Id: RCV000015331 RCV000084544 RCV000995804
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_058519.3:p.Ser637Phe
CA225475
NM_016835.5:c.1910C>T