Canonical Allele Identifier: PA2826636152
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 821214
ClinVar RCV Id: RCV001015405 RCV001860791 RCV003492205
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Val498Ile
CA068922
NM_001281494.2:c.1492G>A