Canonical Allele Identifier: PA2499290382
Gene: RNASEH2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1058489
ClinVar RCV Id: RCV001367637
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078846.2:p.Trp73Cys
CA388258849
NM_024570.4:c.219G>C
CA388258850
NM_024570.4:c.219G>T