Canonical Allele Identifier: PA2580336965
Gene: SOS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1740268

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008870.2:p.Asn147Asp
CA389649596
NM_006939.4:c.439A>G