Canonical Allele Identifier: PA645493906
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 427045

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079492.2:p.Gly221Arg
CA2113990
NM_025216.3:c.661G>A
CA350587051
NM_025216.3:c.661G>C