Canonical Allele Identifier: PA2826628244
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2567451
ClinVar RCV Id: RCV003311248
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser937Arg
CA346757863
NM_001281492.2:c.2809A>C
CA346757876
NM_001281492.2:c.2811T>G
CA346757878
NM_001281492.2:c.2811T>A