Canonical Allele Identifier: PA2826635745
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483772
ClinVar RCV Id: RCV000561829 RCV001315932
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ala402Val
CA346750947
NM_001281494.2:c.1205C>T