Canonical Allele Identifier: PA2826631921
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410521
ClinVar RCV Id: RCV000759137 RCV000470821 RCV000491946 RCV004001855
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ile570Val
CA16611154
NM_001281493.2:c.1708A>G