Canonical Allele Identifier: PA658749505
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 490005
ClinVar RCV Id: RCV000580926
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu1187Gln
CA346760411
NM_000179.3:c.3559G>C