Canonical Allele Identifier: PA103299
Gene: TPP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 68743
ClinVar RCV Id: RCV000059625
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000382.3:p.Pro544Ser
CA266186
NM_000391.4:c.1630C>T