Canonical Allele Identifier: PA645421307
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 225318

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542411.2:p.Gly230Trp
CA3751596
NM_080680.3:c.688G>T