Canonical Allele Identifier: PA136131
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40716

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Asn1011Ser
CA136129
NM_005633.4:c.3032A>G