Canonical Allele Identifier: PA2828703759
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14247
ClinVar RCV Id: RCV000015316 RCV000084554 RCV002476970
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364195.1:p.Arg701Trp
CA225495
NM_001377266.1:c.2101C>T