Canonical Allele Identifier: PA2830356504
Gene: SIX5 HGNC NCBI

Linked Data

ClinVar Variation Id: 3162588
ClinVar RCV Id: RCV004455987

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_787071.3:p.Ser333Phe
CA309000972
NM_175875.5:c.998C>T