Canonical Allele Identifier: PA2580316338
Gene: SIX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2026219
ClinVar RCV Id: RCV002871248

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005973.1:p.Met1Ile
CA389911253
NM_005982.4:c.3G>T
CA389911254
NM_005982.4:c.3G>C
CA389911255
NM_005982.4:c.3G>A