Canonical Allele Identifier: PA645381274
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410423
ClinVar RCV Id: RCV000471001 RCV000479094 RCV000766575 RCV002418411 RCV003470463
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys660Gln
CA16610909
NM_000179.3:c.1978A>C