Canonical Allele Identifier: PA2830130299
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 178812
ClinVar RCV Id: RCV000155584 RCV000261111 RCV000301208 RCV000353712 RCV000368741 RCV000477787 RCV001651028 RCV003907479
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542410.2:p.Asn1204Ser
CA183082
NM_080679.3:c.3611A>G