Canonical Allele Identifier: PA182753
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 178663

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542411.2:p.Glu1628Asp
CA182752
NM_080680.3:c.4884G>C
CA363616585
NM_080680.3:c.4884G>T