Canonical Allele Identifier: PA1139763240
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 989509
ClinVar RCV Id: RCV001277358
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079492.2:p.Arg388Cys
CA350592125
NM_025216.3:c.1162C>T