ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826264607
Gene: MAPT
HGNC
NCBI
Linked Data
ClinVar Variation Id:
14259
ClinVar RCV Id:
RCV000015328
RCV000084515
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001190180.1:p.Lys228Thr
CA225413
NM_001203251.2:c.683A>C