Canonical Allele Identifier: PA2826723465
Gene: USP7 HGNC NCBI

Linked Data

ClinVar Variation Id: 440942
ClinVar RCV Id: RCV000509482 RCV001175170
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273386.2:p.Met209Ile
CA394704278
NM_001286457.2:c.627G>T
CA394704279
NM_001286457.2:c.627G>C
CA394704280
NM_001286457.2:c.627G>A