Canonical Allele Identifier: PA916011343
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142482
ClinVar RCV Id: RCV000131620 RCV003758697
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ala934Thr
CA011817
NM_001281492.2:c.2800G>A