Canonical Allele Identifier: PA2828703726
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14262
ClinVar RCV Id: RCV000015331 RCV000084544 RCV000995804
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364195.1:p.Ser615Phe
CA225475
NM_001377266.1:c.1844C>T