Canonical Allele Identifier: PA658680786
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455167
ClinVar RCV Id: RCV000534112 RCV000569127 RCV003488656 RCV004003668
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gln657Arg
CA346750602
NM_000179.3:c.1970A>G