Canonical Allele Identifier: PA2830159401
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 178927
ClinVar RCV Id: RCV000155702 RCV000709936 RCV000680469 RCV001154083 RCV001154084 RCV001537799 RCV001154085
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542412.2:p.Ala888Val
CA183327
NM_080681.3:c.2663C>T