ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825588891
Gene: MAPT
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000015324
RCV000084553
RCV000517183
RCV001851871
ClinVar Variation:
14255
98232
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001116539.1:p.Gly360Arg
CA225494
NM_001123067.4:c.1078G>C
CA257189
NM_001123067.4:c.1078G>A