Canonical Allele Identifier: PA2499296015
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1224337
ClinVar RCV Id: RCV001596875

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542411.2:p.Thr1611Ser
CA363617484
NM_080680.3:c.4832C>G
CA363617488
NM_080680.3:c.4831A>T