Canonical Allele Identifier: PA163999
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 140948
ClinVar RCV Id: RCV000129224 RCV001294307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser292Ile
CA016579
NM_000179.3:c.875G>T