Canonical Allele Identifier: PA2828703729
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_001364195.1:p.Gly630Ser
CA225477
NM_001377266.1:c.1888G>A