Canonical Allele Identifier: PA259607
Gene: CHN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 29623
ClinVar RCV Id: RCV000022463
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001813.1:p.Pro141Leu
CA259606
NM_001822.7:c.422C>T