Canonical Allele Identifier: PA658666932
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 464180
ClinVar RCV Id: RCV000558141 RCV001829581
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079492.2:p.Met72Ile
CA2113862
NM_025216.3:c.216G>T
CA350618542
NM_025216.3:c.216G>A
CA350618544
NM_025216.3:c.216G>C