Canonical Allele Identifier: PA2826636651
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 480919
ClinVar RCV Id: RCV000561147 RCV000590239 RCV000793228 RCV003459309 RCV004000907
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ala613Gly
CA346755403
NM_001281494.2:c.1838C>G