Canonical Allele Identifier: PA2826085734
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 2092717
ClinVar RCV Id: RCV003018339
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166896.1:p.Asn559His
CA5205857
NM_001173425.1:c.1675A>C