Canonical Allele Identifier: PA2830158743
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 356409

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542412.2:p.Glu287Asp
CA10626491
NM_080681.3:c.861G>C
CA363609336
NM_080681.3:c.861G>T