Canonical Allele Identifier: PA2826636899
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142327
ClinVar RCV Id: RCV000131393 RCV000212673 RCV000630013 RCV001355155 RCV001818325 RCV003462013 RCV003998102
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Arg674Cys
CA011096
NM_001281494.2:c.2020C>T