Canonical Allele Identifier: PA645421420
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 286092
ClinVar RCV Id: RCV000296836 RCV001156809 RCV001156810 RCV001156808
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542411.2:p.Glu767Gly
CA3750958
NM_080680.3:c.2300A>G