Canonical Allele Identifier: PA2826931947
Gene: RNF32 HGNC NCBI

Linked Data

ClinVar Variation Id: 3155404
ClinVar RCV Id: RCV004446733
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295202.1:p.Lys268Ile
CA370147589
NM_001308273.2:c.803A>T