Canonical Allele Identifier: PA2826636544
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 439203
ClinVar RCV Id: RCV000506119 RCV000794150 RCV001179711 RCV004003551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Leu591Val
CA069423
NM_001281494.2:c.1771C>G