Canonical Allele Identifier: PA2826264679
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14261
ClinVar RCV Id: RCV000015330 RCV000266864
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001190181.1:p.Arg5His
CA257191
NM_001203252.2:c.14G>A