Canonical Allele Identifier: PA2826633532
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_001268422.1:p.Glu932_Leu933dup
CA645369302
NM_001281493.2:c.2795_2800dup