Canonical Allele Identifier: PA296832
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181349
ClinVar RCV Id: RCV000158807 RCV000213209 RCV000622058 RCV003317105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Met493Val
CA010805
NM_000257.4:c.1477A>G