Canonical Allele Identifier: PA2573074227
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14253
ClinVar RCV Id: RCV000015322 RCV000084521 RCV000763404
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364194.1:p.Asn671Lys
CA225424
NM_001377265.1:c.2013T>G
CA399983169
NM_001377265.1:c.2013T>A