Canonical Allele Identifier: PA2826634803
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2676814
ClinVar RCV Id: RCV003470254 RCV004011327
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Thr186Ala
CA067704
NM_001281494.2:c.556A>G