Canonical Allele Identifier: PA2826628671
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2587342
ClinVar RCV Id: RCV003360820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ala1074Val
CA346760572
NM_001281492.2:c.3221C>T