Canonical Allele Identifier: PA2826585334
Gene: RNF214 HGNC NCBI
ClinVar RCV:
RCV004446630
ClinVar Variation:
3155301
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265178.1:p.Ser27Pro
CA6293305
NM_001278249.2:c.79T>C