Canonical Allele Identifier: PA658747988
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 491936
ClinVar RCV Id: RCV000582599 RCV000708887 RCV000807532 RCV003459447
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Phe1103Val
CA346758568
NM_000179.3:c.3307T>G