Canonical Allele Identifier: PA645384472
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428304
ClinVar RCV Id: RCV000491347 RCV000502171
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu1234_Leu1235dup
CA645369302
NM_000179.3:c.3701_3706dup