ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826264797
Gene: MAPT
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
104100
ClinVar RCV:
RCV000084513
RCV000325065
RCV000805364
RCV003935077
RCV003993800
ClinVar Variation:
98208
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001190181.1:p.Ala239Thr
CA225409
NM_001203252.2:c.715G>A