Canonical Allele Identifier: PA117697
Gene: RNF6 HGNC NCBI

Linked Data

ClinVar Variation Id: 5701
ClinVar RCV Id: RCV000006055

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005968.1:p.Ala242Thr
CA117696
NM_005977.4:c.724G>A