Canonical Allele Identifier: PA916012016
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 823910
ClinVar RCV Id: RCV001020575 RCV002550862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ile881Met
CA346760264
NM_001281494.2:c.2643A>G