Canonical Allele Identifier: PA2826635270
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127564
ClinVar RCV Id: RCV000115383 RCV000233835 RCV000409692 RCV000562745 RCV001800402 RCV003997237
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Phe294Ile
CA009191
NM_001281494.2:c.880T>A