Canonical Allele Identifier: PA2573252078
Gene: SOS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1385905
ClinVar RCV Id: RCV001889048

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008870.2:p.Thr1091Ser
CA389640464
NM_006939.4:c.3272C>G
CA389640467
NM_006939.4:c.3271A>T