Canonical Allele Identifier: PA2830160083
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2161737
ClinVar RCV Id: RCV003078723
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542412.2:p.Pro1529Ser
CA363617448
NM_080681.3:c.4585C>T