Canonical Allele Identifier: PA2826084974
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 517373
ClinVar RCV Id: RCV000613409 RCV001067423 RCV001168206 RCV001168205
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166896.1:p.Thr47Ala
CA5206357
NM_001173425.1:c.139A>G