Canonical Allele Identifier: PA127092
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 17123
ClinVar RCV Id: RCV000018660
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542410.2:p.Gly1334Glu
CA127091
NM_080679.3:c.4001G>A