Canonical Allele Identifier: PA110475
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 18369
ClinVar RCV Id: RCV000020037
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000742.1:p.Phe95Leu
CA128069
NM_000751.2:c.283T>C
CA350997468
NM_000751.2:c.285T>A
CA350997469
NM_000751.2:c.285T>G