Canonical Allele Identifier: PA2741878383
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 2772507
ClinVar RCV Id: RCV003516088
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364194.1:p.Gln699His
CA399983428
NM_001377265.1:c.2097A>C
CA399983429
NM_001377265.1:c.2097A>T