Canonical Allele Identifier: PA174378
Gene: ZNF48 HGNC NCBI

Linked Data

ClinVar Variation Id: 161575
ClinVar RCV Id: RCV000149110
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001201838.1:p.Pro542Ser
CA174377
NM_001214909.2:c.1624C>T