Canonical Allele Identifier: PA658744299
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 491989
ClinVar RCV Id: RCV000582921
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile225Thr
CA346739440
NM_000179.3:c.674T>C