Canonical Allele Identifier: PA174176
Gene: ZNF419 HGNC NCBI

Linked Data

ClinVar Variation Id: 161512
ClinVar RCV Id: RCV000149046

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091964.1:p.Gly26Cys
CA174175
NM_001098494.2:c.76G>T