Canonical Allele Identifier: PA103367
Gene: TPP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 556797
ClinVar RCV Id: RCV000672851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000382.3:p.Trp548Arg
CA379472034
NM_000391.4:c.1642T>C
CA379472035
NM_000391.4:c.1642T>A