Canonical Allele Identifier: PA2826631688
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 953307
ClinVar RCV Id: RCV001225578
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Pro514Ser
CA346754060
NM_001281493.2:c.1540C>T