Canonical Allele Identifier: PA645417743
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_060525.3:p.Arg248Trp
CA16618976
NM_018055.5:c.742C>T