Canonical Allele Identifier: PA2828704032
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14262
ClinVar RCV Id: RCV000015331 RCV000084544 RCV000995804
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364197.1:p.Ser231Phe
CA225475
NM_001377268.1:c.692C>T