Canonical Allele Identifier: PA183083
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 178812
ClinVar RCV Id: RCV000155584 RCV000261111 RCV000301208 RCV000353712 RCV000368741 RCV000477787 RCV001651028 RCV003907479
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542411.2:p.Asn1311Ser
CA183082
NM_080680.3:c.3932A>G