Canonical Allele Identifier: PA1139680202
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 935357
ClinVar RCV Id: RCV001203928
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000742.1:p.Glu430Asp
CA351005562
NM_000751.2:c.1290A>C
CA351005564
NM_000751.2:c.1290A>T