Canonical Allele Identifier: PA2826629911
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 582516
ClinVar RCV Id: RCV000706608
ClinVar Variation Id: 1403905
ClinVar RCV Id: RCV001898894 RCV002344002 RCV003442947
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Val96Leu
CA067302
NM_001281493.2:c.286G>T
CA346743374
NM_001281493.2:c.286G>C