Allele Registry

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Canonical Allele Identifier: PA2825091975

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 653382

ClinVar RCV Id: RCV000809152

ClinVar Variation Id: 940856

ClinVar RCV Id: RCV001210530 RCV002460136

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Val1212Leu	CA346760609 NM_000179.3:c.3634G>C CA346760610 NM_000179.3:c.3634G>T