Canonical Allele Identifier: PA2826630687
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 834778
ClinVar RCV Id: RCV001035529 RCV002409357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Thr282Ser
CA346748961
NM_001281493.2:c.844A>T
CA346748965
NM_001281493.2:c.845C>G