Canonical Allele Identifier: PA136167
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40654
ClinVar RCV Id: RCV000038563 RCV000624181 RCV000466303 RCV004018718
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Val171Gly
CA136165
NM_005633.4:c.512T>G