Canonical Allele Identifier: PA275519
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 203387
ClinVar RCV Id: RCV000185565 RCV000185564 RCV000216709 RCV000415812 RCV001375279 RCV003947558
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056219.3:p.Pro676Arg
CA275518
NM_015404.4:c.2027C>G