Canonical Allele Identifier: PA2826632102
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455216
ClinVar RCV Id: RCV000560703 RCV000566003 RCV000708881 RCV001558112 RCV003459170
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Arg609Gln
CA069556
NM_001281493.2:c.1826G>A