Canonical Allele Identifier: PA2826631557
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 480921
ClinVar RCV Id: RCV000571434 RCV000695468
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Asn482Lys
CA346753538
NM_001281493.2:c.1446C>A
CA346753543
NM_001281493.2:c.1446C>G