Canonical Allele Identifier: PA2825085237
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 963713
ClinVar RCV Id: RCV001237778 RCV003584872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly45Ser
CA46688123
NM_000179.3:c.133G>A