Canonical Allele Identifier: PA2830129671
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 218349
ClinVar RCV Id: RCV000202578
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542410.2:p.Pro781Thr
CA248587
NM_080679.3:c.2341C>A