Canonical Allele Identifier: PA2826628514
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483828
ClinVar RCV Id: RCV000562398 RCV003593987
ClinVar Variation Id: 1732205
ClinVar RCV Id: RCV002459261
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg1042Ser
CA346760202
NM_001281492.2:c.3126A>T
CA346760203
NM_001281492.2:c.3126A>C