Canonical Allele Identifier: PA2826636196
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1497344
ClinVar RCV Id: RCV001992335 RCV002458958
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Leu509Ile
CA346754030
NM_001281494.2:c.1525C>A