Canonical Allele Identifier: PA2825111113
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2563041

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asn754Asp
CA389048802
NM_000257.4:c.2260A>G