Canonical Allele Identifier: PA2580470773
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 2279150
ClinVar RCV Id: RCV002827591
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079492.2:p.Leu64Phe
CA350618403
NM_025216.3:c.192G>C
CA350618405
NM_025216.3:c.192G>T