Allele Registry

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Canonical Allele Identifier: PA2826636049

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 495707

ClinVar RCV Id: RCV000587268 RCV000772486 RCV000821395

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Gln474His	CA346753318 NM_001281494.2:c.1422A>C CA346753321 NM_001281494.2:c.1422A>T