Canonical Allele Identifier: PA916070918
Gene: SIX5 HGNC NCBI

Linked Data

ClinVar Variation Id: 224344
ClinVar RCV Id: RCV000416581
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_787071.3:p.Val421Ile
CA16044141
NM_175875.5:c.1261G>A