Canonical Allele Identifier: PA916056908
Gene: COL11A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 291519

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542197.3:p.Pro961Thr
CA974092
NM_080630.4:c.2881C>A