Canonical Allele Identifier: PA658680020
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483762
ClinVar RCV Id: RCV000564219 RCV001349167 RCV004001046
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala53Asp
CA346734958
NM_000179.3:c.158C>A