Canonical Allele Identifier: PA916011946
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89400
ClinVar RCV Id: RCV000074868 RCV000121587 RCV000132123 RCV000587729 RCV001084016 RCV001137560 RCV001353894 RCV003149723
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Glu861Val
CA013119
NM_001281494.2:c.2582A>T