Canonical Allele Identifier: PA2826631294
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 143007
ClinVar RCV Id: RCV000132526 RCV000469296 RCV001201355 RCV003462049 RCV003320574
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Arg419Gly
CA009782
NM_001281493.2:c.1255A>G