Canonical Allele Identifier: PA1139743106
Gene: CHN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17552
ClinVar RCV Id: RCV000019107
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358443.1:p.Tyr160His
CA258036
NM_001371514.1:c.478T>C