Canonical Allele Identifier: PA645427127
Gene: SIX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 418491
ClinVar RCV Id: RCV000483984

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005973.1:p.Glu183Gly
CA16619880
NM_005982.4:c.548A>G