Allele Registry

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Canonical Allele Identifier: PA916012118

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428287

ClinVar RCV Id: RCV000491503 RCV001851334

ClinVar Variation Id: 801704

ClinVar RCV Id: RCV000986740 RCV002346194 RCV003467542

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Gly914Arg	CA346760635 NM_001281494.2:c.2740G>A CA346760636 NM_001281494.2:c.2740G>C