Canonical Allele Identifier: PA658663194
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 454364

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Thr1062Ser
CA389045274
NM_000257.4:c.3185C>G
CA389045277
NM_000257.4:c.3184A>T