Allele Registry

Canonical Allele Identifier: PA2573300967

Gene: COL11A2 HGNC NCBI

ClinVar RCV:

RCV001949715

ClinVar Variation:

1426358

HGVS (amino-acid)	Matching Registered Transcripts
NP_542411.2:p.Pro445Ser	CA363606167 NM_080680.3:c.1333C>T