Canonical Allele Identifier: PA2826627350
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 232501
ClinVar RCV Id: RCV000220336 RCV000691459
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu688Phe
CA10578106
NM_001281492.2:c.2062C>T