Canonical Allele Identifier: PA136185
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40660
ClinVar RCV Id: RCV000038569 RCV000157705 RCV000228572 RCV001261072 RCV001813282 RCV002390135 RCV003944869
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Val250Ala
CA136183
NM_005633.4:c.749T>C