Allele Registry

Canonical Allele Identifier: PA2580503417

Gene: COL11A2 HGNC NCBI

ClinVar RCV:

RCV002908974

ClinVar Variation:

2045887

HGVS (amino-acid)	Matching Registered Transcripts
NP_542411.2:p.Thr1620Met	CA3749986 NM_080680.3:c.4859C>T