Canonical Allele Identifier: PA2830160099
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1361179
ClinVar RCV Id: RCV001865126

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542412.2:p.Ser1544Phe
CA3749961
NM_080681.3:c.4631C>T