Canonical Allele Identifier: PA2825088738
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2682020
ClinVar RCV Id: RCV003477312
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys598Asn
CA346749308
NM_000179.3:c.1794A>T
CA346749310
NM_000179.3:c.1794A>C