Canonical Allele Identifier: PA2573163519
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1525371
ClinVar RCV Id: RCV002036634
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Phe706Ile
CA346750964
NM_000179.3:c.2116T>A