Allele Registry

Canonical Allele Identifier: PA2741993682

Gene: HMCN1 HGNC NCBI

ClinVar RCV:

RCV003708871

ClinVar Variation:

2816559

HGVS (amino-acid)	Matching Registered Transcripts
NP_114141.2:p.Val1620Ala	CA343885918 NM_031935.3:c.4859T>C