Canonical Allele Identifier: PA2826635730
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 232785
ClinVar RCV Id: RCV000218126 RCV000232938 RCV000684784 RCV002478805
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Leu398Ile
CA10578092
NM_001281494.2:c.1192C>A