Canonical Allele Identifier: PA2826586849
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1714899
ClinVar RCV Id: RCV002304429 RCV002352974
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ala1004Thr
CA346761452
NM_001281494.2:c.3010G>A