Canonical Allele Identifier: PA645384711
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410391
ClinVar RCV Id: RCV002230101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val1271Ile
CA16610950
NM_000179.3:c.3811G>A