Canonical Allele Identifier: PA916057491
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 391897
ClinVar RCV Id: RCV000437358 RCV000764646
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542410.2:p.Thr990Pro
CA3750574
NM_080679.3:c.2968A>C