Canonical Allele Identifier: PA2825111764
Gene: MYH7 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asn897His
CA034040
NM_000257.4:c.2689A>C