Canonical Allele Identifier: PA2830129694
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 356398
ClinVar RCV Id: RCV000290480 RCV000344614 RCV000379273 RCV000400234 RCV001538789
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542410.2:p.Gly788Ala
CA3750764
NM_080679.3:c.2363G>C