Canonical Allele Identifier: PA645421444
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 356396
ClinVar RCV Id: RCV000282164 RCV000283442 RCV000337227 RCV000391260 RCV001770281
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542411.2:p.Pro950Ser
CA3750711
NM_080680.3:c.2848C>T