Canonical Allele Identifier: PA330553
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89445
ClinVar RCV Id: RCV000217680 RCV000574037 RCV000625244 RCV001854284
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile1227Leu
CA013789
NM_000179.3:c.3679A>T
CA346760894
NM_000179.3:c.3679A>C