Canonical Allele Identifier: PA913198390
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 632997

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Asn485Ser
CA45674752
NM_005633.4:c.1454A>G