Canonical Allele Identifier: PA2826633422
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428285
ClinVar RCV Id: RCV000491433 RCV003449281 RCV004003451 RCV002523978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu907Pro
CA346760597
NM_001281493.2:c.2720T>C