Canonical Allele Identifier: PA915989133
Gene: HES7 HGNC NCBI

Linked Data

ClinVar Variation Id: 30697
ClinVar RCV Id: RCV001807738
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159439.1:p.Asp191Tyr
CA129404
NM_001165967.2:c.571G>T