Canonical Allele Identifier: PA2826626001
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455143
ClinVar RCV Id: RCV000537542 RCV000574659 RCV003459167 RCV004003663
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg377Gly
CA346746363
NM_001281492.2:c.1129A>G