Allele Registry

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Canonical Allele Identifier: PA2826633911

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455307

ClinVar RCV Id: RCV000547026 RCV001186971

ClinVar Variation Id: 525638

ClinVar RCV Id: RCV000629765 RCV003237961 RCV002377344

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Asn1005Lys	CA346761460 NM_001281493.2:c.3015T>G CA346761461 NM_001281493.2:c.3015T>A