Canonical Allele Identifier: PA645378887
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410477
ClinVar RCV Id: RCV002230117
ClinVar Variation Id: 1422451
ClinVar RCV Id: RCV001945615
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile251Leu
CA16611116
NM_000179.3:c.751A>T
CA346740125
NM_000179.3:c.751A>C