Canonical Allele Identifier: PA225457
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_001116538.2:p.Ser640Asn
CA225453
NM_001123066.4:c.1919G>A