Canonical Allele Identifier: PA2829358446
Gene: HDC HGNC NCBI

Linked Data

ClinVar Variation Id: 3104658
ClinVar RCV Id: RCV004401516
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002103.2:p.Thr577Ser
CA7554508
NM_002112.4:c.1729A>T
CA392377191
NM_002112.4:c.1730C>G