Canonical Allele Identifier: PA2826631065
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 924818
ClinVar RCV Id: RCV001186405
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ile367Val
CA068352
NM_001281493.2:c.1099A>G