Canonical Allele Identifier: PA658680690
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 485855
ClinVar RCV Id: RCV000575004

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile570Leu
CA346748557
NM_000179.3:c.1708A>C
CA346748563
NM_000179.3:c.1708A>T