Canonical Allele Identifier: PA2573295075
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1433900
ClinVar RCV Id: RCV001960204

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542411.2:p.Val1625Met
CA3749963
NM_080680.3:c.4873G>A