Allele Registry

Canonical Allele Identifier: PA2830130687

Gene: COL11A2 HGNC NCBI

ClinVar RCV:

RCV000294143

RCV000295270

RCV000352446

RCV000391825

RCV000498284

RCV000766647

RCV003401372

ClinVar Variation:

356383

HGVS (amino-acid)	Matching Registered Transcripts
NP_542410.2:p.Arg1444Trp	CA3750029 NM_080679.3:c.4330C>T