Canonical Allele Identifier: PA2828893387
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 180719
ClinVar RCV Id: RCV000157695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Pro474Leu
CA235355
NM_001382394.1:c.1421C>T