Canonical Allele Identifier: PA658666951
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 464179
ClinVar RCV Id: RCV000537520
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079492.2:p.Cys404Trp
CA350592627
NM_025216.3:c.1212C>G