Canonical Allele Identifier: PA2827275098
Gene: NODAL HGNC NCBI

Linked Data

ClinVar Variation Id: 418388
ClinVar RCV Id: RCV000482914
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316835.1:p.Arg115Trp
CA16618976
NM_001329906.2:c.343C>T