Canonical Allele Identifier: PA2826634647
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89189
ClinVar RCV Id: RCV000074651 RCV000491070 RCV000627730 RCV000576688 RCV003466933 RCV001804803 RCV003137604
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Leu147Pro
CA008516
NM_001281494.2:c.440T>C
CA2850447133
NM_001281494.2:c.438_440delinsCCC