Canonical Allele Identifier: PA2826631395
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 948777
ClinVar RCV Id: RCV001220101 RCV002418756 RCV003462747
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Asn446Ser
CA346752616
NM_001281493.2:c.1337A>G