Canonical Allele Identifier: PA2829646311
Gene: SRSF6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3170282
ClinVar RCV Id: RCV004460712

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006266.2:p.Arg233Gly
CA409071311
NM_006275.6:c.697C>G