Canonical Allele Identifier: PA2573074234
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14268
ClinVar RCV Id: RCV000015338 RCV000084543
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364194.1:p.Lys709Met
CA225473
NM_001377265.1:c.2126A>T