Canonical Allele Identifier: PA2827386639
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 45662
ClinVar RCV Id: RCV000038880 RCV001213992
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333819.1:p.Val215Leu
CA136896
NM_001346890.1:c.643G>C
CA374621112
NM_001346890.1:c.643G>T