Canonical Allele Identifier: PA658653940
Gene: SIX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 444331
ClinVar RCV Id: RCV000512900 RCV000706990 RCV001375398 RCV002524959
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005973.1:p.Arg64His
CA261723226
NM_005982.4:c.191G>A