Canonical Allele Identifier: PA916012227
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 647730
ClinVar RCV Id: RCV000802298 RCV001021080
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asp953His
CA346761108
NM_001281494.2:c.2857G>C