Canonical Allele Identifier: PA136909
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_056219.3:p.Gly765Arg
CA136908
NM_015404.4:c.2293G>C