Canonical Allele Identifier: PA2741993682
Gene: HMCN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2816559
ClinVar RCV Id: RCV003708871
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114141.2:p.Val1620Ala
CA343885918
NM_031935.3:c.4859T>C