Canonical Allele Identifier: PA2830158730
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 198609
ClinVar RCV Id: RCV000223442 RCV000678342 RCV000764647 RCV000724260 RCV001253705 RCV002277425
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542412.2:p.Gly271Ser
CA247358
NM_080681.3:c.811G>A