Canonical Allele Identifier: PA2580337704
Gene: SOX5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2444597
ClinVar RCV Id: RCV003154116

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008871.3:p.Met1Ile
CA384321302
NM_006940.6:c.3G>T
CA384321303
NM_006940.6:c.3G>C
CA384321304
NM_006940.6:c.3G>A