Canonical Allele Identifier: PA2826162042
Gene: COL11A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 197911

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177638.1:p.Val1232Leu
CA246297
NM_001190709.2:c.3694G>T
CA341162107
NM_001190709.2:c.3694G>C