Canonical Allele Identifier: PA252134
Gene: MYH14 HGNC NCBI
ClinVar RCV:
RCV000002281
ClinVar Variation:
2197
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139281.1:p.Leu1017Phe
CA252133
NM_001145809.2:c.3049C>T