Canonical Allele Identifier: PA645384419
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 420856
ClinVar RCV Id: RCV000483707 RCV000581141 RCV000809551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala1226Thr
CA16617706
NM_000179.3:c.3676G>A