Canonical Allele Identifier: PA2830158531
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2881782
ClinVar RCV Id: RCV003708286
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542411.2:p.Glu229Asp
CA363610344
NM_080680.3:c.687G>C
CA363610345
NM_080680.3:c.687G>T