Canonical Allele Identifier: PA2830158200
Gene: COL11A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1349520
ClinVar RCV Id: RCV002051089
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542196.2:p.Pro1089Ala
CA341171091
NM_080629.3:c.3265C>G