Canonical Allele Identifier: PA2830160121
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1371300

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542412.2:p.Val1565Phe
CA363616281
NM_080681.3:c.4693G>T