Canonical Allele Identifier: PA1139689365
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 923359
ClinVar RCV Id: RCV001183945
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser41Phe
CA346734872
NM_001281492.2:c.122C>T