Canonical Allele Identifier: PA2573284124
Gene: RNASEH2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1410990
ClinVar RCV Id: RCV001920388
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078846.2:p.His213Gln
CA388259819
NM_024570.4:c.639T>A
CA388259820
NM_024570.4:c.639T>G