Canonical Allele Identifier: PA2826626757
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 489975
ClinVar RCV Id: RCV000580872 RCV002304216 RCV004001264
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu548Gly
CA346750727
NM_001281492.2:c.1643A>G