Canonical Allele Identifier: PA658654125
Gene: SOS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 445827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008870.2:p.Leu672Ile
CA7177182
NM_006939.4:c.2014C>A