Canonical Allele Identifier: PA2826587325
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 220943
ClinVar RCV Id: RCV000205455 RCV000217289 RCV000519500 RCV001711360 RCV003997660
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asn1025Ser
CA072431
NM_001281494.2:c.3074A>G