Canonical Allele Identifier: PA225427
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14253
ClinVar RCV Id: RCV000015322 RCV000084521 RCV000763404
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005901.2:p.Asn279Lys
CA225424
NM_005910.6:c.837T>G
CA399983169
NM_005910.6:c.837T>A