Canonical Allele Identifier: PA2826284638
Gene: CHN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 29624
ClinVar RCV Id: RCV000022464
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193531.1:p.Pro127Ser
CA259608
NM_001206602.1:c.379C>T