Allele Registry

Canonical Allele Identifier: PA2580468337

Gene: HMCN1 HGNC NCBI

ClinVar RCV:

RCV002603870

ClinVar Variation:

1919404

HGVS (amino-acid)	Matching Registered Transcripts
NP_114141.2:p.His3481Arg	CA1293725 NM_031935.3:c.10442A>G