Canonical Allele Identifier: PA335784
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_000170.1:p.Arg302Lys
CA073568
NM_000179.3:c.905G>A