Canonical Allele Identifier: PA645421481
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 356388
ClinVar RCV Id: RCV000292046 RCV000293307 RCV000352855 RCV000382942 RCV001850900
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542411.2:p.Arg1284Trp
CA10626652
NM_080680.3:c.3850C>T