Canonical Allele Identifier: PA2573265608
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 1516404
ClinVar RCV Id: RCV002040838
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056219.3:p.Phe106Leu
CA374612956
NM_015404.4:c.318C>G
CA374612960
NM_015404.4:c.318C>A
CA374612979
NM_015404.4:c.316T>C