Canonical Allele Identifier: PA2826085422
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 1010617
ClinVar RCV Id: RCV001308272
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166896.1:p.Arg381Ser
CA5206072
NM_001173425.1:c.1143G>C
CA374609891
NM_001173425.1:c.1143G>T