Canonical Allele Identifier: PA645493900
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 379584
ClinVar RCV Id: RCV000431228

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079492.2:p.Asp217Gly
CA16604387
NM_025216.3:c.650A>G