Canonical Allele Identifier: PA2826636212
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428397
ClinVar RCV Id: RCV000490982 RCV001851341
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Leu513Arg
CA069080
NM_001281494.2:c.1538T>G