Canonical Allele Identifier: PA1139690779
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 925470
ClinVar RCV Id: RCV001187439 RCV003594115
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Leu875Ile
CA346760226
NM_001281494.2:c.2623C>A