Canonical Allele Identifier: PA2826161359
Gene: COL11A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 291537
ClinVar RCV Id: RCV000282658 RCV000337630 RCV001859738
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177638.1:p.Thr355Ala
CA975103
NM_001190709.2:c.1063A>G