Canonical Allele Identifier: PA2826628952
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2587348
ClinVar RCV Id: RCV003350672 RCV003777494
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu1134Val
CA346761178
NM_001281492.2:c.3400C>G