Canonical Allele Identifier: PA2826631598
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2747363
ClinVar RCV Id: RCV003593635
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Asp491Gly
CA346753732
NM_001281493.2:c.1472A>G