Canonical Allele Identifier: PA2825086551
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1426375
ClinVar RCV Id: RCV001931264
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser219Arg
CA346739325
NM_000179.3:c.655A>C
CA346739334
NM_000179.3:c.657T>A
CA346739336
NM_000179.3:c.657T>G