Canonical Allele Identifier: PA2826631175
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89248
ClinVar RCV Id: RCV000822642 RCV001186406 RCV003450940
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Cys392Arg
CA009656
NM_001281493.2:c.1174T>C