Canonical Allele Identifier: PA2825084919
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 847995
ClinVar RCV Id: RCV001051650
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Tyr8Phe
CA346734501
NM_000179.3:c.23A>T