Canonical Allele Identifier: PA2826635629
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 628496
ClinVar RCV Id: RCV000772969
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ser375Arg
CA346750717
NM_001281494.2:c.1123A>C
CA346750722
NM_001281494.2:c.1125T>G
CA346750723
NM_001281494.2:c.1125T>A