Canonical Allele Identifier: PA2826630638
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428315
ClinVar RCV Id: RCV000491403 RCV001204099
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Gln270Glu
CA346748599
NM_001281493.2:c.808C>G