Canonical Allele Identifier: PA225455
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14254
ClinVar RCV Id: RCV000015323 RCV000084530
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116539.1:p.Ser276Asn
CA225453
NM_001123067.4:c.827G>A