Canonical Allele Identifier: PA2573308542
Gene: SIX5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1466053
ClinVar RCV Id: RCV001959406
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_787071.3:p.Pro513Ser
CA406417516
NM_175875.5:c.1537C>T