Canonical Allele Identifier: PA2825092043
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1493059
ClinVar RCV Id: RCV001984084
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp1223Asn
CA346760845
NM_000179.3:c.3667G>A