Canonical Allele Identifier: PA916012004
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 577926
ClinVar RCV Id: RCV000700791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Gly876Ser
CA346760231
NM_001281494.2:c.2626G>A