Canonical Allele Identifier: PA225478
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 98228
ClinVar RCV Id: RCV000084545 RCV003514309
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_058519.3:p.Gly652Ser
CA225477
NM_016835.5:c.1954G>A