Canonical Allele Identifier: PA2499229343
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1171916
ClinVar RCV Id: RCV001525377
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu819Gly
CA346754081
NM_000179.3:c.2456A>G