Canonical Allele Identifier: PA225445
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14245
ClinVar RCV Id: RCV000015313 RCV000084527 RCV000763405 RCV002508757 RCV003407335
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_058518.1:p.Pro243Leu
CA225444
NM_016834.5:c.728C>T