Canonical Allele Identifier: PA1139765143
Gene: RAI1 HGNC NCBI

Linked Data

ClinVar Variation Id: 930437
ClinVar RCV Id: RCV001196096

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109590.3:p.Thr207Ser
CA398545856
NM_030665.4:c.619A>T
CA398545858
NM_030665.4:c.620C>G