Canonical Allele Identifier: PA916010922
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 490023
ClinVar RCV Id: RCV000580185 RCV000629974
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser18Arg
CA346734549
NM_001281492.2:c.52A>C
CA346734554
NM_001281492.2:c.54T>A
CA346734555
NM_001281492.2:c.54T>G