Canonical Allele Identifier: PA2827651197
Gene: RCBTB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 253017
ClinVar RCV Id: RCV000239602 RCV000258140 RCV001090333
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339435.1:p.Trp117Cys
CA6982735
NM_001352506.2:c.351G>T
CA388189781
NM_001352506.2:c.351G>C