Canonical Allele Identifier: PA195722
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 186739
ClinVar RCV Id: RCV000166383 RCV000629923
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro1087Leu
CA012288
NM_000179.3:c.3260C>T