Canonical Allele Identifier: PA2826633927
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 490014
ClinVar RCV Id: RCV000580869 RCV003117349
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Pro1007Leu
CA346761473
NM_001281493.2:c.3020C>T