Canonical Allele Identifier: PA2826085580
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 45654
ClinVar RCV Id: RCV000038872 RCV000888343 RCV001165874 RCV001165873
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166896.1:p.Pro485Leu
CA136881
NM_001173425.1:c.1454C>T