Canonical Allele Identifier: PA658654620
Gene: USP7 HGNC NCBI

Linked Data

ClinVar Variation Id: 440942

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003461.2:p.Met225Ile
CA394704278
NM_003470.3:c.675G>T
CA394704279
NM_003470.3:c.675G>C
CA394704280
NM_003470.3:c.675G>A