Canonical Allele Identifier: PA127093
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_542412.2:p.Gly1355Glu
CA127091
NM_080681.3:c.4064G>A