Canonical Allele Identifier: PA2830158414
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2793131
ClinVar RCV Id: RCV003667670

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542411.2:p.Val1645Ala
CA363616360
NM_080680.3:c.4934T>C