Canonical Allele Identifier: PA102019
Gene: SIX3 HGNC NCBI

Linked Data

ClinVar Variation Id: 6099
ClinVar RCV Id: RCV000006472 RCV000506131
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005404.1:p.Trp113Cys
CA253773
NM_005413.4:c.339G>T
CA346799364
NM_005413.4:c.339G>C