Canonical Allele Identifier: PA2830130798
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 178663

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542410.2:p.Glu1521Asp
CA182752
NM_080679.3:c.4563G>C
CA363616585
NM_080679.3:c.4563G>T