Canonical Allele Identifier: PA645383694
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 420757
ClinVar RCV Id: RCV000484206 RCV001019455 RCV001303106 RCV004003333
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr1085Ile
CA16617694
NM_000179.3:c.3254C>T