Canonical Allele Identifier: PA2830130890
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1437721
ClinVar RCV Id: RCV001957663

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542410.2:p.Arg1560Cys
CA3749939
NM_080679.3:c.4678C>T