Canonical Allele Identifier: PA2826161606
Gene: COL11A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 291526

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177638.1:p.Pro635Ser
CA974667
NM_001190709.2:c.1903C>T