Canonical Allele Identifier: PA2826808340
Gene: ZNF419 HGNC NCBI

Linked Data

ClinVar Variation Id: 161512
ClinVar RCV Id: RCV000149046

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278674.1:p.Gly13Cys
CA174175
NM_001291745.1:c.37G>T