Canonical Allele Identifier: PA2826631471
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455186
ClinVar RCV Id: RCV000549148 RCV004003674 RCV003237888 RCV002456039
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Cys463Ser
CA346752969
NM_001281493.2:c.1387T>A
CA346752975
NM_001281493.2:c.1388G>C