Canonical Allele Identifier: PA2826637515
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 660233
ClinVar RCV Id: RCV002325607 RCV000817387
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Gly814Ser
CA346758747
NM_001281494.2:c.2440G>A