Canonical Allele Identifier: PA915977326
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14247
ClinVar RCV Id: RCV000015316 RCV000084554 RCV002476970
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116538.2:p.Arg741Trp
CA225495
NM_001123066.4:c.2221C>T