Canonical Allele Identifier: PA2826631908
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1024913
ClinVar RCV Id: RCV001325153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Met566Leu
CA346754931
NM_001281493.2:c.1696A>C
CA346754934
NM_001281493.2:c.1696A>T