Canonical Allele Identifier: PA2825088092
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1717044
ClinVar RCV Id: RCV002296230
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu446Gln
CA346744560
NM_000179.3:c.1336G>C