Canonical Allele Identifier: PA2828704034
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 98228
ClinVar RCV Id: RCV000084545 RCV003514309
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364197.1:p.Gly246Ser
CA225477
NM_001377268.1:c.736G>A