Canonical Allele Identifier: PA2826635991
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410460
ClinVar RCV Id: RCV000477003 RCV004022783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asp461Gly
CA16610931
NM_001281494.2:c.1382A>G