Canonical Allele Identifier: PA2580157469
Gene: RRM2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1908106
ClinVar RCV Id: RCV002581306
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165948.1:p.Asn415Ile
CA371585277
NM_001172477.1:c.1244A>T