Canonical Allele Identifier: PA2828703563
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_001364195.1:p.Arg5His
CA257191
NM_001377266.1:c.14G>A