Canonical Allele Identifier: PA658654126
Gene: SOS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 445735

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008870.2:p.Ile1252del
CA7176713
NM_006939.4:c.3755_3757del