Canonical Allele Identifier: PA100430
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 98215
ClinVar RCV Id: RCV000084524
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_058519.3:p.Asn613His
CA225433
NM_016835.5:c.1837A>C