Canonical Allele Identifier: PA2826625589
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410392
ClinVar RCV Id: RCV000520334 RCV000460255 RCV000567415 RCV004000828
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asn274Ser
CA067350
NM_001281492.2:c.821A>G