Canonical Allele Identifier: PA2825087145
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2567494
ClinVar RCV Id: RCV003311268
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser287Arg
CA346740584
NM_000179.3:c.859A>C
CA346740593
NM_000179.3:c.861T>A
CA346740595
NM_000179.3:c.861T>G