ClinGen Allele Registry
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Canonical Allele Identifier:
PA2829854927
Gene: MAPT
HGNC
NCBI
Linked Data
ClinVar Variation Id:
14262
ClinVar RCV Id:
RCV000015331
RCV000084544
RCV000995804
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_058518.1:p.Ser262Phe
CA225475
NM_016834.5:c.785C>T