Canonical Allele Identifier: PA128793
Gene: CHRDL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 29958
ClinVar RCV Id: RCV000022850

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137453.1:p.Cys261Phe
CA128792
NM_001143981.2:c.782G>T