Canonical Allele Identifier: PA2826635757
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455177
ClinVar RCV Id: RCV000549707 RCV002420343
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Glu405Gly
CA346750986
NM_001281494.2:c.1214A>G