Canonical Allele Identifier: PA1139743105
Gene: CHN1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358443.1:p.Pro158Leu
CA259606
NM_001371514.1:c.473C>T