Canonical Allele Identifier: PA2826626730
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410451
ClinVar RCV Id: RCV000470045 RCV000491796 RCV001565312 RCV004001833 RCV003463933
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Pro543Ala
CA068368
NM_001281492.2:c.1627C>G