Allele Registry

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Canonical Allele Identifier: PA2826634635

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89188

ClinVar RCV Id: RCV000074650

ClinVar Variation Id: 2859099

ClinVar RCV Id: RCV003759249

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Glu144Asp	CA008501 NM_001281494.2:c.432A>T CA346744577 NM_001281494.2:c.432A>C