Canonical Allele Identifier: PA225440
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_058518.1:p.Pro243Ser
CA225439
NM_016834.5:c.727C>T