Allele Registry

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Canonical Allele Identifier: PA100471

Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14255

ClinVar RCV Id: RCV000517183 RCV001851871 RCV000015324

ClinVar Variation Id: 98232

ClinVar RCV Id: RCV000084553

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_058519.3:p.Gly706Arg	CA225494 NM_016835.5:c.2116G>C CA257189 NM_016835.5:c.2116G>A