Canonical Allele Identifier: PA2826631512
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 419439
ClinVar RCV Id: RCV000483513 RCV003758786
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu471Val
CA16617671
NM_001281493.2:c.1411C>G