Canonical Allele Identifier: PA2827386547
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 504565
ClinVar RCV Id: RCV000611623 RCV001049406 RCV001165877 RCV001165878
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333819.1:p.Met110Leu
CA5205980
NM_001346890.1:c.328A>C
CA374608498
NM_001346890.1:c.328A>T