Allele Registry

Canonical Allele Identifier: PA2830128885

Gene: COL11A2 HGNC NCBI

ClinVar RCV:

RCV001949715

ClinVar Variation:

1426358

HGVS (amino-acid)	Matching Registered Transcripts
NP_542410.2:p.Pro338Ser	CA363606167 NM_080679.3:c.1012C>T