Canonical Allele Identifier: PA2580395653
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 1929399
ClinVar RCV Id: RCV002642369

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056219.3:p.Gly757Arg
CA5205677
NM_015404.4:c.2269G>A
CA374619940
NM_015404.4:c.2269G>C