Canonical Allele Identifier: PA2826636005
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_001268423.1:p.His464Arg
CA16610933
NM_001281494.2:c.1391A>G