Canonical Allele Identifier: PA2828703430
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_001364194.1:p.Pro215Ser
CA8617674
NM_001377265.1:c.643C>T