Canonical Allele Identifier: PA645387588
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411867

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Pro1255Thr
CA16610833
NM_005633.4:c.3763C>A