Canonical Allele Identifier: PA2826636169
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 571392
ClinVar RCV Id: RCV000692527 RCV002458235
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ile503Met
CA346753997
NM_001281494.2:c.1509C>G