Canonical Allele Identifier: PA2826635573
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1784018
ClinVar RCV Id: RCV002416955
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Glu363Gln
CA346750653
NM_001281494.2:c.1087G>C