Canonical Allele Identifier: PA2826624923
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 140780
ClinVar RCV Id: RCV000128926 RCV000168003 RCV000202238 RCV000410809 RCV000656890 RCV000761137 RCV003492580 RCV003467099
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Val120Ala
CA016410
NM_001281492.2:c.359T>C