Canonical Allele Identifier: PA2826635050
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 418743
ClinVar RCV Id: RCV000479973 RCV000545794 RCV000574287 RCV000765683 RCV000659891 RCV003470532 RCV004002268
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Lys243Glu
CA16617656
NM_001281494.2:c.727A>G