Canonical Allele Identifier: PA2828491660
Gene: CHN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17550
ClinVar RCV Id: RCV000019105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358442.1:p.Leu20Phe
CA258034
NM_001371513.1:c.60A>T
CA349689277
NM_001371513.1:c.60A>C