Canonical Allele Identifier: PA2826085009
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 1480670
ClinVar RCV Id: RCV002022119
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166896.1:p.Asp73Glu
CA374613623
NM_001173425.1:c.219C>G
CA374613626
NM_001173425.1:c.219C>A