Canonical Allele Identifier: PA915977271
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14268
ClinVar RCV Id: RCV000015338 RCV000084543
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116538.2:p.Lys652Met
CA225473
NM_001123066.4:c.1955A>T