Canonical Allele Identifier: PA2830159730
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 356387
ClinVar RCV Id: RCV000264819 RCV000323351 RCV000322375 RCV000383939 RCV001850899 RCV002487566
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542412.2:p.Glu1209Lys
CA3750325
NM_080681.3:c.3625G>A