Canonical Allele Identifier: PA2826634299
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1023014
ClinVar RCV Id: RCV001323000
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Gln23Leu
CA346740976
NM_001281494.2:c.68A>T