Canonical Allele Identifier: PA891865608
Gene: DLX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 591644
ClinVar RCV Id: RCV000722825
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_612138.1:p.Leu204_Trp205delinsHisArg
CA891863077
NM_138281.3:c.611_613delinsACA