Canonical Allele Identifier: PA2830159002
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 17129

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542412.2:p.Pro535Thr
CA212599
NM_080681.3:c.1603C>A