Canonical Allele Identifier: PA281697
Gene: COL11A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17131
ClinVar RCV Id: RCV000018669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542196.2:p.Gly637Val
CA281694
NM_080629.3:c.1910G>T