Allele Registry

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Canonical Allele Identifier: PA658680787

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479971

ClinVar RCV Id: RCV000574848 RCV001227127 RCV003492101 RCV004000888

ClinVar Variation Id: 2837716

ClinVar RCV Id: RCV003758378

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gln657His	CA346750604 NM_000179.3:c.1971G>C CA346750605 NM_000179.3:c.1971G>T