Canonical Allele Identifier: PA2826086029
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 1929399
ClinVar RCV Id: RCV002642369
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166896.1:p.Gly756Arg
CA5205677
NM_001173425.1:c.2266G>A
CA374619940
NM_001173425.1:c.2266G>C