Canonical Allele Identifier: PA225496
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_005901.2:p.Arg406Trp
CA225495
NM_005910.6:c.1216C>T