Canonical Allele Identifier: PA2826635591
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 234550
ClinVar RCV Id: RCV000219193 RCV000562974 RCV001054199
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ser366Pro
CA10577271
NM_001281494.2:c.1096T>C