Canonical Allele Identifier: PA2830130854
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1392771
ClinVar RCV Id: RCV001882262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542410.2:p.Val1544Ala
CA363616275
NM_080679.3:c.4631T>C