Canonical Allele Identifier: PA645417695
Gene: NODAL HGNC NCBI

Linked Data

ClinVar Variation Id: 300311
ClinVar RCV Id: RCV000350811 RCV000372771
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060525.3:p.Val68Ala
CA10635597
NM_018055.5:c.203T>C