Canonical Allele Identifier: PA645384651
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428336
ClinVar RCV Id: RCV000491950 RCV000629866 RCV001284183 RCV004003455
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Tyr1256Ser
CA071991
NM_000179.3:c.3767A>C