Canonical Allele Identifier: PA645470947
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 424385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157243.1:p.Pro289Ser
CA3751572
NM_001163771.2:c.865C>T