Canonical Allele Identifier: PA259609
Gene: CHN1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001813.1:p.Pro252Ser
CA259608
NM_001822.7:c.754C>T