Canonical Allele Identifier: PA2826637569
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1171608
ClinVar RCV Id: RCV001524841 RCV001872052
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ala825Val
CA346758821
NM_001281494.2:c.2474C>T