Canonical Allele Identifier: PA2826633406
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 823994
ClinVar RCV Id: RCV001020734
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ala904Ser
CA346760580
NM_001281493.2:c.2710G>T