Canonical Allele Identifier: PA658680982
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455200
ClinVar RCV Id: RCV000524653 RCV003302770
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg820Lys
CA346754086
NM_000179.3:c.2459G>A