Canonical Allele Identifier: PA645416598
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 423459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ile988Ser
CA16619848
NM_000257.4:c.2963T>G