Canonical Allele Identifier: PA2830129270
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 356403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542410.2:p.Gly578Ala
CA10626490
NM_080679.3:c.1733G>C