Canonical Allele Identifier: PA2826635497
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3073290
ClinVar RCV Id: RCV004015304
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ser346Gly
CA46709970
NM_001281494.2:c.1036A>G