Canonical Allele Identifier: PA2828704018
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_001364197.1:p.Leu208Val
CA225417
NM_001377268.1:c.622C>G