Canonical Allele Identifier: PA658805336
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 506216
ClinVar RCV Id: RCV000610034
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542411.2:p.His1648Leu
CA363616329
NM_080680.3:c.4943A>T