Canonical Allele Identifier: PA102409
Gene: WNT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 50262
ClinVar RCV Id: RCV000043497 RCV000678662
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005421.1:p.Val355Phe
CA143728
NM_005430.4:c.1063G>T