Canonical Allele Identifier: PA106618
Gene: SIX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 420132
ClinVar RCV Id: RCV000482613 RCV003223408
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005973.1:p.Arg110Gln
CA16619881
NM_005982.4:c.329G>A