Canonical Allele Identifier: PA2829854845
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_058518.1:p.Leu208Val
CA225417
NM_016834.5:c.622C>G