Canonical Allele Identifier: PA2826161430
Gene: COL11A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 291535
ClinVar RCV Id: RCV000275597 RCV000330638 RCV000494431
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177638.1:p.Arg437His
CA974978
NM_001190709.2:c.1310G>A