Canonical Allele Identifier: PA1139674635
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 945630
ClinVar RCV Id: RCV001216312
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser718Arg
CA346751114
NM_000179.3:c.2152A>C
CA346751122
NM_000179.3:c.2154C>A
CA346751123
NM_000179.3:c.2154C>G