Canonical Allele Identifier: PA2830160108
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1386535
ClinVar RCV Id: RCV001905804

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542412.2:p.Arg1555Trp
CA363616412
NM_080681.3:c.4663C>T