Canonical Allele Identifier: PA2825091326
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 950452
ClinVar RCV Id: RCV001222165
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val1132Phe
CA346758857
NM_000179.3:c.3394G>T