Canonical Allele Identifier: PA2826635544
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1320382
ClinVar RCV Id: RCV001776361 RCV003759072
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Leu357Phe
CA346750614
NM_001281494.2:c.1069C>T