Canonical Allele Identifier: PA2825112993
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2805702
ClinVar RCV Id: RCV003749374

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.His1553Gln
CA389037913
NM_000257.4:c.4659C>G
CA389037914
NM_000257.4:c.4659C>A