Canonical Allele Identifier: PA2826628879
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 218070
ClinVar RCV Id: RCV000202077 RCV000491301 RCV000533181 RCV000657120 RCV001375485 RCV003462357 RCV003997048
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.His1118_Ser1127del
CA279716
NM_001281492.2:c.3354_3383del