Canonical Allele Identifier: PA2825515430
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_001077354.2:p.Gly382Arg
CA136908
NM_001083885.3:c.1144G>C