Canonical Allele Identifier: PA2825091849
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 951839
ClinVar RCV Id: RCV001223834
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val1192Ala
CA346760502
NM_000179.3:c.3575T>C