Canonical Allele Identifier: PA111825
Gene: PC HGNC NCBI
ClinVar Allele:
17135
ClinVar RCV:
RCV000002177
ClinVar Variation:
2096
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000911.2:p.Val145Ala
CA339940
NM_000920.4:c.434T>C