Canonical Allele Identifier: PA915977221
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 529746
ClinVar RCV Id: RCV000635209 RCV001128500
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116538.2:p.Arg544His
CA8618037
NM_001123066.4:c.1631G>A