Canonical Allele Identifier: PA191119
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 185132
ClinVar RCV Id: RCV000164500 RCV001850300
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu665Gly
CA009517
NM_000179.3:c.1994A>G