Canonical Allele Identifier: PA2580475279
Gene: ZNF442 HGNC NCBI

Linked Data

ClinVar Variation Id: 2490208
ClinVar RCV Id: RCV004273828

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110451.1:p.Gly317Ala
CA404220702
NM_030824.3:c.950G>C