Canonical Allele Identifier: PA2828893351
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2106812

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Met439Ile
CA1624605
NM_001382394.1:c.1317G>T
CA346366394
NM_001382394.1:c.1317G>A
CA346366395
NM_001382394.1:c.1317G>C