Canonical Allele Identifier: PA645382186
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 234760
ClinVar RCV Id: RCV000221553
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg820Met
CA10577274
NM_000179.3:c.2459G>T