Canonical Allele Identifier: PA2573082493
Gene: SOX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1302955
ClinVar RCV Id: RCV001756454

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003097.1:p.Pro253Ala
CA355474588
NM_003106.4:c.757C>G