Allele Registry

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Canonical Allele Identifier: PA2825085269

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1393402

ClinVar RCV Id: RCV001884521 RCV004010790

ClinVar Variation Id: 2700954

ClinVar RCV Id: RCV003594898

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Asp47Glu	CA346734917 NM_000179.3:c.141T>A CA346734919 NM_000179.3:c.141T>G