Canonical Allele Identifier: PA136923
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 45677
ClinVar RCV Id: RCV000038895 RCV000725335 RCV000988244 RCV001168207 RCV001168208
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056219.3:p.Ser11Arg
CA136922
NM_015404.4:c.33C>G
CA374614799
NM_015404.4:c.33C>A
CA374614818
NM_015404.4:c.31A>C