Canonical Allele Identifier: PA2573074230
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14256
ClinVar RCV Id: RCV000015325 RCV000084526
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364194.1:p.Pro693Ser
CA225439
NM_001377265.1:c.2077C>T