Canonical Allele Identifier: PA2826631008
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_001268422.1:p.Gln355Arg
CA346750602
NM_001281493.2:c.1064A>G