Canonical Allele Identifier: PA2830160137
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1371091
ClinVar RCV Id: RCV001878820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542412.2:p.Gly1576Ser
CA363616115
NM_080681.3:c.4726G>A