Canonical Allele Identifier: PA2825112104
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3230904
ClinVar RCV Id: RCV004523018
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gly984Ala
CA389046441
NM_000257.4:c.2951G>C