Allele Registry

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Canonical Allele Identifier: PA2826633235

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483828

ClinVar RCV Id: RCV000562398 RCV003593987

ClinVar Variation Id: 1732205

ClinVar RCV Id: RCV002459261

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Arg870Ser	CA346760202 NM_001281493.2:c.2610A>T CA346760203 NM_001281493.2:c.2610A>C