Canonical Allele Identifier: PA2826587155
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89490
ClinVar RCV Id: RCV000074958 RCV000148646 RCV000115425 RCV000202255 RCV000410058 RCV000590664 RCV001082577 RCV001355442 RCV004528273
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Arg1019Gly
CA014874
NM_001281494.2:c.3055A>G