Canonical Allele Identifier: PA2825089040
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2587354
ClinVar RCV Id: RCV003360828
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu655Phe
CA346750590
NM_000179.3:c.1965A>C
CA346750591
NM_000179.3:c.1965A>T