Canonical Allele Identifier: PA2580440807
Gene: PRDM8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1965606
ClinVar RCV Id: RCV002745310

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064611.3:p.Phe362Leu
CA357398131
NM_020226.4:c.1084T>C
CA357398142
NM_020226.4:c.1086C>A
CA357398143
NM_020226.4:c.1086C>G