Canonical Allele Identifier: PA916011046
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 393459
ClinVar RCV Id: RCV000445517 RCV002411422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ala61Thr
CA16609275
NM_001281492.2:c.181G>A