Canonical Allele Identifier: PA645480338
Gene: HMCN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 294145

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114141.2:p.Thr1480Ile
CA1292003
NM_031935.3:c.4439C>T