Canonical Allele Identifier: PA2826162223
Gene: COL11A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 291500

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177638.1:p.Pro1460Ser
CA973507
NM_001190709.2:c.4378C>T