Canonical Allele Identifier: PA2826636252
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 993195
ClinVar RCV Id: RCV001284515 RCV001370089
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Lys522Glu
CA346754121
NM_001281494.2:c.1564A>G