Allele Registry

Canonical Allele Identifier: PA3057520087

Gene: HMCN1 HGNC NCBI

ClinVar RCV:

RCV005161750

ClinVar Variation:

3684845

HGVS (amino-acid)	Matching Registered Transcripts
NP_114141.2:p.His3481Asp	CA343930701 NM_031935.3:c.10441C>G