Canonical Allele Identifier: PA2573061726
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1332141
ClinVar RCV Id: RCV001804657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys317Thr
CA346740822
NM_000179.3:c.950A>C