Canonical Allele Identifier: PA645381354
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 237150
ClinVar RCV Id: RCV000231201 RCV000772336 RCV003463637 RCV003998714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu675Lys
CA10582057
NM_000179.3:c.2023G>A