Canonical Allele Identifier: PA645421513
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 356383
ClinVar RCV Id: RCV000294143 RCV000295270 RCV000352446 RCV000391825 RCV000498284 RCV000766647 RCV003401372
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542411.2:p.Arg1551Trp
CA3750029
NM_080680.3:c.4651C>T