Canonical Allele Identifier: PA1139671823
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 925648
ClinVar RCV Id: RCV001187730
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala261Val
CA389052064
NM_000257.4:c.782C>T