Canonical Allele Identifier: PA156126
Gene: ZNF407 HGNC NCBI

Linked Data

ClinVar Variation Id: 130822

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060227.2:p.Val143Phe
CA156125
NM_017757.3:c.427G>T