Canonical Allele Identifier: PA916076601
Gene: RNASEH2B HGNC NCBI

Linked Data

ClinVar Variation Id: 645436
ClinVar RCV Id: RCV000799508
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078846.2:p.Lys103Arg
CA6985525
NM_024570.4:c.308A>G