Canonical Allele Identifier: PA357790
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 224582
ClinVar RCV Id: RCV000210111 RCV000217860 RCV000693978 RCV002469072
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg901Ser
CA069480
NM_000179.3:c.2701C>A