Canonical Allele Identifier: PA103391
Gene: TPP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 68749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000382.3:p.Val277Met
CA266191
NM_000391.4:c.829G>A