Canonical Allele Identifier: PA2825088263
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1773239
ClinVar RCV Id: RCV002396813
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro489Ser
CA346745833
NM_000179.3:c.1465C>T