Canonical Allele Identifier: PA2826264719
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 3029792
ClinVar RCV Id: RCV003899049
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001190181.1:p.Gln88His
CA399898315
NM_001203252.2:c.264G>C
CA399898316
NM_001203252.2:c.264G>T