Canonical Allele Identifier: PA2826637389
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 186739
ClinVar RCV Id: RCV000166383 RCV000629923
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Pro785Leu
CA012288
NM_001281494.2:c.2354C>T