Canonical Allele Identifier: PA2499245119
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1034975
ClinVar RCV Id: RCV001337776
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Val951del
CA2496054167
NM_001281494.2:c.2852_2854del