Canonical Allele Identifier: PA122816
Gene: RNASEL HGNC NCBI

Linked Data

ClinVar Variation Id: 13005
ClinVar RCV Id: RCV000013879

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066956.1:p.Met1Ile
CA122815
NM_021133.4:c.3G>A
CA343646405
NM_021133.4:c.3G>T
CA343646406
NM_021133.4:c.3G>C