Canonical Allele Identifier: PA2826635589
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1518110
ClinVar RCV Id: RCV002021505
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ser366Phe
CA46710117
NM_001281494.2:c.1097C>T