Canonical Allele Identifier: PA2830129456
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 286092

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542410.2:p.Glu660Gly
CA3750958
NM_080679.3:c.1979A>G