Canonical Allele Identifier: PA2826264797
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 98208
ClinVar RCV Id: RCV000084513 RCV000325065 RCV000805364 RCV003993800 RCV003935077
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001190181.1:p.Ala239Thr
CA225409
NM_001203252.2:c.715G>A