Canonical Allele Identifier: PA2825089067
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1713432
ClinVar RCV Id: RCV002295462 RCV002416562
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Met662Arg
CA346750635
NM_000179.3:c.1985T>G