Canonical Allele Identifier: PA225476
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005901.2:p.Ser320Phe
CA225475
NM_005910.6:c.959C>T