Allele Registry

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Canonical Allele Identifier: PA645382704

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410385

ClinVar RCV Id: RCV000759140 RCV002230099

ClinVar Variation Id: 801221

ClinVar RCV Id: RCV000985835 RCV002549655

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Trp912Arg	CA16610945 NM_000179.3:c.2734T>C CA346755380 NM_000179.3:c.2734T>A