Canonical Allele Identifier: PA2825112133
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3069440
ClinVar RCV Id: RCV004007984
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1012Thr
CA389045830
NM_000257.4:c.3034G>A