Canonical Allele Identifier: PA2826633897
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89479
ClinVar RCV Id: RCV000074947 RCV000132026 RCV000212691 RCV000524193 RCV000986742 RCV001354037 RCV003149724
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Arg1002Lys
CA014661
NM_001281493.2:c.3005G>A