Canonical Allele Identifier: PA2826637424
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 231691
ClinVar RCV Id: RCV000223169 RCV001067326
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Gly791Arg
CA10578136
NM_001281494.2:c.2371G>A
CA346758291
NM_001281494.2:c.2371G>C