Canonical Allele Identifier: PA2828491696
Gene: CHN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17553
ClinVar RCV Id: RCV000019108
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358442.1:p.Ala223Val
CA258037
NM_001371513.1:c.668C>T