Canonical Allele Identifier: PA658746484
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 491896
ClinVar RCV Id: RCV000582673 RCV000629957
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro802Ser
CA346753942
NM_000179.3:c.2404C>T