Allele Registry

Canonical Allele Identifier: PA3063125084

Gene: HMCN1 HGNC NCBI

ClinVar RCV:

RCV005577120

ClinVar Variation:

4035570

HGVS (amino-acid)	Matching Registered Transcripts
NP_114141.2:p.Thr3483Pro	CA343930732 NM_031935.3:c.10447A>C