Canonical Allele Identifier: PA916051040
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 706054
ClinVar RCV Id: RCV000876539 RCV003948248
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_058519.3:p.Pro140Ser
CA8617674
NM_016835.5:c.418C>T