Canonical Allele Identifier: PA645493865
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 334393

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079492.2:p.Pro50Leu
CA2113843
NM_025216.3:c.149C>T