Canonical Allele Identifier: PA2826630967
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1331853
ClinVar RCV Id: RCV001804369 RCV001869507
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu345Val
CA346750452
NM_001281493.2:c.1033C>G