Canonical Allele Identifier: PA2826634577
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 216294
ClinVar RCV Id: RCV000485339 RCV001312494 RCV002381687 RCV003454502
ClinVar Variation Id: 1769181
ClinVar RCV Id: RCV002380619
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Phe130Leu
CA337394
NM_001281494.2:c.390T>G
CA346744219
NM_001281494.2:c.388T>C
CA346744228
NM_001281494.2:c.390T>A