Canonical Allele Identifier: PA2830160161
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 391128
ClinVar RCV Id: RCV000436866
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542412.2:p.Arg1609Trp
CA3749909
NM_080681.3:c.4825C>T