Canonical Allele Identifier: PA138635
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 46568

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542411.2:p.Pro1722Leu
CA138634
NM_080680.3:c.5165C>T