Canonical Allele Identifier: PA2826631679
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1501691
ClinVar RCV Id: RCV002010774 RCV003170536
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Lys511Asn
CA346754046
NM_001281493.2:c.1533G>C
CA346754047
NM_001281493.2:c.1533G>T