Canonical Allele Identifier: PA645421467
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 356393
ClinVar RCV Id: RCV000260343 RCV000348277 RCV000355182 RCV000405447 RCV001580488
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542411.2:p.Pro1110Ser
CA3750551
NM_080680.3:c.3328C>T