Canonical Allele Identifier: PA2830130779
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1064998
ClinVar RCV Id: RCV001375282
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542410.2:p.Arg1509Met
CA363617432
NM_080679.3:c.4526G>T