Canonical Allele Identifier: PA2573074224
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14266
ClinVar RCV Id: RCV000015336 RCV000084517
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364194.1:p.Leu658Val
CA225417
NM_001377265.1:c.1972C>G