Canonical Allele Identifier: PA225454
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_058518.1:p.Ser247Asn
CA225453
NM_016834.5:c.740G>A