ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2828703886
Gene: MAPT
HGNC
NCBI
Linked Data
ClinVar Variation Id:
98210
ClinVar RCV Id:
RCV000084516
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001364196.1:p.Ile231Val
CA225415
NM_001377267.1:c.691A>G