Canonical Allele Identifier: PA1139736012
Gene: PRDM8 HGNC NCBI

Linked Data

ClinVar Variation Id: 846963
ClinVar RCV Id: RCV001050401

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064611.3:p.Pro342Leu
CA357397812
NM_020226.4:c.1025C>T