Canonical Allele Identifier: PA645383710
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 230897
ClinVar RCV Id: RCV000223078 RCV000699366 RCV003997868
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro1086Arg
CA070524
NM_000179.3:c.3257C>G