Canonical Allele Identifier: PA2826633500
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2828521
ClinVar RCV Id: RCV003758213
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ala926Thr
CA346760908
NM_001281493.2:c.2776G>A