Canonical Allele Identifier: PA2830129380
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 356402
ClinVar RCV Id: RCV000276412 RCV000319359 RCV000333898 RCV000353689 RCV000602277 RCV001559646
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542410.2:p.Ile621Phe
CA3751010
NM_080679.3:c.1861A>T