Canonical Allele Identifier: PA916012381
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410393
ClinVar RCV Id: RCV000477645 RCV000561056 RCV001290552 RCV003477984 RCV004000829
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Lys994Glu
CA16610959
NM_001281494.2:c.2980A>G