Allele Registry

Canonical Allele Identifier: PA2830130785

Gene: COL11A2 HGNC NCBI

ClinVar RCV:

RCV002908974

ClinVar Variation:

2045887

HGVS (amino-acid)	Matching Registered Transcripts
NP_542410.2:p.Thr1513Met	CA3749986 NM_080679.3:c.4538C>T