Canonical Allele Identifier: PA127088
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 17121
ClinVar RCV Id: RCV000018658 RCV001851920
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542410.2:p.Gly554Arg
CA127087
NM_080679.3:c.1660G>A
CA3751090
NM_080679.3:c.1660G>C