Canonical Allele Identifier: PA2826634286
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 628592
ClinVar RCV Id: RCV000773124 RCV000810970
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ala20Val
CA346740919
NM_001281494.2:c.59C>T