Canonical Allele Identifier: PA645381863
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410386
ClinVar RCV Id: RCV000574487 RCV002230403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.His766Arg
CA16610933
NM_000179.3:c.2297A>G