Canonical Allele Identifier: PA351535
Gene: TPP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 221282
ClinVar RCV Id: RCV000207147
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000382.3:p.Arg152Ser
CA351534
NM_000391.4:c.456G>C
CA217323938
NM_000391.4:c.456G>T