Canonical Allele Identifier: PA2828491701
Gene: CHN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 29624
ClinVar RCV Id: RCV000022464

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358442.1:p.Pro252Ser
CA259608
NM_001371513.1:c.754C>T