Canonical Allele Identifier: PA2826629884
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455119
ClinVar RCV Id: RCV000529516 RCV001010152 RCV003320670
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ala91Gly
CA067262
NM_001281493.2:c.272C>G