Allele Registry

Canonical Allele Identifier: PA2580467717

Gene: HMCN1 HGNC NCBI

ClinVar RCV:

RCV002576913

ClinVar Variation:

1901361

HGVS (amino-acid)	Matching Registered Transcripts
NP_114141.2:p.Met1589Ile	CA33453531 NM_031935.3:c.4767G>T CA343885134 NM_031935.3:c.4767G>A CA343885136 NM_031935.3:c.4767G>C