Canonical Allele Identifier: PA2826631742
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 651137
ClinVar RCV Id: RCV000806430 RCV003353039
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Val526Leu
CA346754178
NM_001281493.2:c.1576G>C