Canonical Allele Identifier: PA2573062037
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1333641
ClinVar RCV Id: RCV001808857
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ile511Leu
CA389050387
NM_000257.4:c.1531A>C