Canonical Allele Identifier: PA2499229283
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1019926
ClinVar RCV Id: RCV001319430
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gln244His
CA346740042
NM_000179.3:c.732A>C
CA346740044
NM_000179.3:c.732A>T