Canonical Allele Identifier: PA2826635017
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2433804
ClinVar RCV Id: RCV003132686
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Tyr236Phe
CA346747031
NM_001281494.2:c.707A>T