Allele Registry

Canonical Allele Identifier: PA212611

Gene: COL11A2 HGNC NCBI

ClinVar RCV:

RCV000148342

RCV000202598

RCV003556192

ClinVar Variation:

160366

HGVS (amino-acid)	Matching Registered Transcripts
NP_542411.2:p.Ala37Ser	CA212610 NM_080680.3:c.109G>T