Canonical Allele Identifier: PA2830530604
Gene: RNF214 HGNC NCBI
ClinVar RCV:
RCV004446630
ClinVar Variation:
3155301
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997226.2:p.Ser27Pro
CA6293305
NM_207343.4:c.79T>C