Canonical Allele Identifier: PA2825108857
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2664345
ClinVar RCV Id: RCV003445446

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala196Gly
CA389052473
NM_000257.4:c.587C>G