Canonical Allele Identifier: PA257192
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_005901.2:p.Arg5His
CA257191
NM_005910.6:c.14G>A