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