Canonical Allele Identifier: PA2830159804
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 162981
ClinVar RCV Id: RCV000150349 RCV000764645 RCV001560335
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542412.2:p.Pro1261Gln
CA175561
NM_080681.3:c.3782C>A