Canonical Allele Identifier: PA2573098320
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1311729
ClinVar RCV Id: RCV001752712

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542411.2:p.Gly1657Val
CA363616183
NM_080680.3:c.4970G>T