Canonical Allele Identifier: PA2826264838
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 98231
ClinVar RCV Id: RCV000084551 RCV000692998 RCV003905079
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001190181.1:p.Val332Ile
CA225490
NM_001203252.2:c.994G>A