Canonical Allele Identifier: PA2830130884
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2003129
ClinVar RCV Id: RCV002825115

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542410.2:p.Leu1557Arg
CA363616082
NM_080679.3:c.4670T>G