Canonical Allele Identifier: PA1139753966
Gene: HMCN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 876514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114141.2:p.Val1184Ala
CA1291764
NM_031935.3:c.3551T>C