Canonical Allele Identifier: PA2826636207
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 953436
ClinVar RCV Id: RCV001225729 RCV003994237
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Lys511Arg
CA346754044
NM_001281494.2:c.1532A>G