Canonical Allele Identifier: PA916011838
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 489959
ClinVar RCV Id: RCV000579921 RCV000629996
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Thr93Ala
CA346742386
NM_001281494.2:c.277A>G