Canonical Allele Identifier: PA2826636170
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483861
ClinVar RCV Id: RCV000571872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ile503Phe
CA346753989
NM_001281494.2:c.1507A>T