Canonical Allele Identifier: PA2573062064
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1316721

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ser241Phe
CA389052184
NM_000257.4:c.722C>T