Canonical Allele Identifier: PA2573165186
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1508961
ClinVar RCV Id: RCV002040554
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp1652Ala
CA389037260
NM_000257.4:c.4955A>C