Canonical Allele Identifier: PA2826636148
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1007727
ClinVar RCV Id: RCV001304954 RCV003166727
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Met497Leu
CA346753874
NM_001281494.2:c.1489A>C
CA346753879
NM_001281494.2:c.1489A>T