Canonical Allele Identifier: PA2826626902
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 232999
ClinVar RCV Id: RCV000221120 RCV000525574 RCV000997142 RCV003462507 RCV003998019
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asp583Asn
CA10578093
NM_001281492.2:c.1747G>A