Canonical Allele Identifier: PA1139675229
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 953436
ClinVar RCV Id: RCV001225729 RCV003994237
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys813Arg
CA346754044
NM_000179.3:c.2438A>G