Canonical Allele Identifier: PA2573295080
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1361179
ClinVar RCV Id: RCV001865126

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542411.2:p.Ser1630Phe
CA3749961
NM_080680.3:c.4889C>T