Allele Registry

Canonical Allele Identifier: PA645412230

Gene: COL11A1 HGNC NCBI

ClinVar Variation Id: 291495

HGVS (amino-acid)	Matching Registered Transcripts
NP_542196.2:p.Asn1614Ser	CA973405 NM_080629.3:c.4841A>G