Canonical Allele Identifier: PA2825085360
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2698888
ClinVar RCV Id: RCV003594849
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly54Glu
CA346734968
NM_000179.3:c.161G>A