Canonical Allele Identifier: PA2829854932
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 98228
ClinVar RCV Id: RCV000084545 RCV003514309
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_058518.1:p.Gly277Ser
CA225477
NM_016834.5:c.829G>A