Canonical Allele Identifier: PA2825088072
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1769836
ClinVar RCV Id: RCV002385619
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala440Ser
CA346744422
NM_000179.3:c.1318G>T