Canonical Allele Identifier: PA658679974
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483760
ClinVar RCV Id: RCV000573405 RCV000703961 RCV004001045
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu30Gln
CA346734813
NM_000179.3:c.88G>C