Canonical Allele Identifier: PA1139736032
Gene: PRDM8 HGNC NCBI

Linked Data

ClinVar Variation Id: 841305
ClinVar RCV Id: RCV001043501
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064611.3:p.Gly363Arg
CA357398146
NM_020226.4:c.1087G>C