Canonical Allele Identifier: PA2826631440
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 439202
ClinVar RCV Id: RCV000506265 RCV001182960 RCV001865651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu456Val
CA346752834
NM_001281493.2:c.1366C>G