Canonical Allele Identifier: PA2826085396
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 177752
ClinVar RCV Id: RCV000154365 RCV000964640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166896.1:p.His364Arg
CA180702
NM_001173425.1:c.1091A>G