Canonical Allele Identifier: PA2828893397
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1360083
ClinVar RCV Id: RCV001864877
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Lys486Asn
CA346366081
NM_001382394.1:c.1458G>T
CA346366082
NM_001382394.1:c.1458G>C