Canonical Allele Identifier: PA2826636197
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 844103
ClinVar RCV Id: RCV001046871 RCV002451187
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Leu509Phe
CA346754032
NM_001281494.2:c.1525C>T