Canonical Allele Identifier: PA2573192718
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1424193
ClinVar RCV Id: RCV001921464 RCV002460174
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Val908Met
CA346760599
NM_001281494.2:c.2722G>A