Canonical Allele Identifier: PA916011568
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455108
ClinVar RCV Id: RCV000540175
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ala37Pro
CA067026
NM_001281494.2:c.109G>C