Canonical Allele Identifier: PA916012193
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89450
ClinVar RCV Id: RCV000074918 RCV000129144 RCV000255857 RCV000524185 RCV001249986 RCV001532986 RCV002243694 RCV003460690
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Arg940del
CA013989
NM_001281494.2:c.2818_2820del