Canonical Allele Identifier: PA645480480
Gene: HMCN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 294200

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114141.2:p.Ile2930Thr
CA1293223
NM_031935.3:c.8789T>C