Canonical Allele Identifier: PA215053
Gene: SIX6 HGNC NCBI

Linked Data

ClinVar Variation Id: 189378
ClinVar RCV Id: RCV000169774
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031400.2:p.Leu37Pro
CA215052
NM_007374.3:c.110T>C