Canonical Allele Identifier: PA645416592
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 312906

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Thr979Arg
CA10643997
NM_000257.4:c.2936C>G