Canonical Allele Identifier: PA2830356502
Gene: SIX5 HGNC NCBI

Linked Data

ClinVar Variation Id: 3162587
ClinVar RCV Id: RCV004455986

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_787071.3:p.Ser319Phe
CA9520708
NM_175875.5:c.956C>T