Canonical Allele Identifier: PA2829855425
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 2772507
ClinVar RCV Id: RCV003516088
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_058519.3:p.Gln624His
CA399983428
NM_016835.5:c.1872A>C
CA399983429
NM_016835.5:c.1872A>T