Canonical Allele Identifier: PA2826161147
Gene: COL11A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 93968

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177638.1:p.Thr72Ser
CA221845
NM_001190709.2:c.215C>G
CA341168601
NM_001190709.2:c.214A>T