Canonical Allele Identifier: PA2826633930
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483785
ClinVar RCV Id: RCV000569784 RCV001070287 RCV003387887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu1008Lys
CA346761475
NM_001281493.2:c.3022G>A