Canonical Allele Identifier: PA2826162365
Gene: COL11A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 291492
ClinVar RCV Id: RCV000265566 RCV000361283 RCV002061149
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177638.1:p.Pro1629Leu
CA973347
NM_001190709.2:c.4886C>T