Canonical Allele Identifier: PA098295
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42950

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gly1057Ser
CA013436
NM_000257.4:c.3169G>A