Canonical Allele Identifier: PA658804403
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 524955
ClinVar RCV Id: RCV000628872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ser260Thr
CA389052075
NM_000257.4:c.778T>A