Canonical Allele Identifier: PA345334
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89187
ClinVar RCV Id: RCV000213558 RCV000627712 RCV000568557 RCV003997065
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile442Thr
CA008493
NM_000179.3:c.1325T>C