Allele Registry

Canonical Allele Identifier: PA916057783

Gene: COL11A2 HGNC NCBI

ClinVar RCV:

RCV000274780

RCV000294955

RCV000317488

RCV000389201

RCV000596294

ClinVar Variation:

356395

HGVS (amino-acid)	Matching Registered Transcripts
NP_542412.2:p.Pro945Leu	CA3750643 NM_080681.3:c.2834C>T CA645548072 NM_080681.3:c.2833_2834delinsTT