Canonical Allele Identifier: PA2826625142
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 216324
ClinVar RCV Id: RCV000195580 RCV000219538 RCV000521245 RCV000845040 RCV003997004
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg172Lys
CA073568
NM_001281492.2:c.515G>A