Canonical Allele Identifier: PA1139724921
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 913731
ClinVar RCV Id: RCV001167515 RCV001167516 RCV001303970
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056219.3:p.Asp358Asn
CA5206089
NM_015404.4:c.1072G>A