Canonical Allele Identifier: PA916012284
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 824257
ClinVar RCV Id: RCV001021223 RCV001861012 RCV004004611
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asn971Ser
CA072186
NM_001281494.2:c.2912A>G