Canonical Allele Identifier: PA2826086046
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 45670
ClinVar RCV Id: RCV000038888
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166896.1:p.Gly764Arg
CA136908
NM_001173425.1:c.2290G>C