Canonical Allele Identifier: PA2826629232
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 234901
ClinVar RCV Id: RCV000221062 RCV001205042 RCV002354622 RCV003333744
ClinVar Variation Id: 433930
ClinVar RCV Id: RCV000501588
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly1186Arg
CA072354
NM_001281492.2:c.3556G>C
CA346761515
NM_001281492.2:c.3556G>A