Canonical Allele Identifier: PA238819
Gene: SIX3 HGNC NCBI

Linked Data

ClinVar Variation Id: 193312
ClinVar RCV Id: RCV000173374 RCV002054049
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005404.1:p.Gly69dup
CA238818
NM_005413.4:c.205_207dup