Canonical Allele Identifier: PA645387258
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 280922
ClinVar RCV Id: RCV000353861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Glu458Asp
CA10602848
NM_005633.4:c.1374G>C
CA346366319
NM_005633.4:c.1374G>T