Canonical Allele Identifier: PA136859
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 45641
ClinVar RCV Id: RCV000886961 RCV001165949 RCV001165950 RCV000038859
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056219.3:p.Arg379Trp
CA136858
NM_015404.4:c.1135C>T