ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826264765
Gene: MAPT
HGNC
NCBI
Linked Data
ClinVar Variation Id:
98205
ClinVar RCV Id:
RCV000084510
RCV000246861
RCV000387650
RCV001079276
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001190181.1:p.Ala178Thr
CA225403
NM_001203252.2:c.532G>A