Canonical Allele Identifier: PA2826632419
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127576
ClinVar RCV Id: RCV000115397 RCV000221869 RCV000558179 RCV000662547 RCV001731378 RCV003997244
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Thr685Ile
CA011210
NM_001281493.2:c.2054C>T