Canonical Allele Identifier: PA2825088396
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1775540
ClinVar RCV Id: RCV002392620

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser525Arg
CA346746803
NM_000179.3:c.1573A>C
CA346746821
NM_000179.3:c.1575T>A
CA346746822
NM_000179.3:c.1575T>G