Canonical Allele Identifier: PA645378393
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 229725
ClinVar RCV Id: RCV000214442 RCV000589961 RCV000629813 RCV000708853 RCV000986701 RCV003462406
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile120Thr
CA071457
NM_000179.3:c.359T>C