Canonical Allele Identifier: PA2829628096
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_005901.2:p.Gln307His
CA399983428
NM_005910.6:c.921A>C
CA399983429
NM_005910.6:c.921A>T