Canonical Allele Identifier: PA2828703917
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 3123393
ClinVar RCV Id: RCV004408763
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364197.1:p.Gly19Arg
CA8617506
NM_001377268.1:c.55G>A
CA291105333
NM_001377268.1:c.55G>C