Allele Registry

Canonical Allele Identifier: PA2580469141

Gene: HMCN1 HGNC NCBI

ClinVar Variation Id: 2187627

HGVS (amino-acid)	Matching Registered Transcripts
NP_114141.2:p.Phe5181Leu	CA1295290 NM_031935.3:c.15541T>C CA343930590 NM_031935.3:c.15543T>A CA343930592 NM_031935.3:c.15543T>G