Canonical Allele Identifier: PA2573295077
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1357906
ClinVar RCV Id: RCV001863943

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542411.2:p.Ser1627Ala
CA363616607
NM_080680.3:c.4879T>G