Canonical Allele Identifier: PA2825088137
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2676816
ClinVar RCV Id: RCV003461948
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Trp456Cys
CA346744884
NM_000179.3:c.1368G>C
CA346744888
NM_000179.3:c.1368G>T