Canonical Allele Identifier: PA2826629553
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1767051
ClinVar RCV Id: RCV002374044 RCV003774182 RCV004007287
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Arg14Gly
CA346740797
NM_001281493.2:c.40A>G