Canonical Allele Identifier: PA2830160024
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 356383
ClinVar RCV Id: RCV000294143 RCV000295270 RCV000352446 RCV000391825 RCV000498284 RCV000766647 RCV003401372
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542412.2:p.Arg1465Trp
CA3750029
NM_080681.3:c.4393C>T