Canonical Allele Identifier: PA136082
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 45347
ClinVar RCV Id: RCV000038518
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Gln477Lys
CA136080
NM_005633.4:c.1429C>A